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Items: 1 to 20 of 19268

1.

rs1491578747 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    CA>- [Show Flanks]
    Chromosome:
    4:75682414 (GRCh38)
    4:76607598 (GRCh37)
    Canonical SPDI:
    NC_000004.12:75682413:CA:
    Gene:
    G3BP2 (Varview)
    Functional Consequence:
    intron_variant,genic_upstream_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    -=0.00017/2 (ALFA)
    HGVS:

    2.

    rs1491572550 has merged into rs34007469 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA [Show Flanks]
      Chromosome:
      4:75720514 (GRCh38)
      4:76645698 (GRCh37)
      Canonical SPDI:
      NC_000004.12:75720501:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:75720501:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:75720501:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:75720501:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:75720501:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:75720501:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:75720501:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
      Gene:
      G3BP2 (Varview)
      Functional Consequence:
      intron_variant,genic_upstream_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AAAAAAAAAAAAA=0./0 (ALFA)
      -=0.2414/141 (NorthernSweden)
      -=0.352/1763 (1000Genomes)
      HGVS:

      3.

      rs1491549072 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        CA>- [Show Flanks]
        Chromosome:
        4:75719347 (GRCh38)
        4:76644531 (GRCh37)
        Canonical SPDI:
        NC_000004.12:75719346:CA:
        Gene:
        G3BP2 (Varview)
        Functional Consequence:
        intron_variant,genic_upstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        -=0.02445/290 (ALFA)
        -=0.00056/1 (Korea1K)
        -=0.00895/148 (TOMMO)
        HGVS:

        4.

        rs1491533480 has merged into rs6148524 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ATATATATATAT>-,AT,ATAT,ATATAT,ATATATAT,ATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATACATATATATATATATATATATATAT,ATATATATATATATATAGATATATATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAGATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATAT,ATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATAGATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT [Show Flanks]
          Chromosome:
          4:75643305 (GRCh38)
          4:76568489 (GRCh37)
          Canonical SPDI:
          NC_000004.12:75643295:TATATATATATATATATATAT:TATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATACATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATAGATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATAGATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATAGATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000004.12:75643295:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
          Gene:
          G3BP2 (Varview)
          Functional Consequence:
          3_prime_UTR_variant,non_coding_transcript_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TATATATATAT=0./0 (ALFA)
          -=0.0192/74 (ALSPAC)
          TA=0.2562/1283 (1000Genomes)
          -=0.4/12 (GENOME_DK)
          HGVS:
          NC_000004.12:g.75643297AT[4], NC_000004.12:g.75643297AT[5], NC_000004.12:g.75643297AT[6], NC_000004.12:g.75643297AT[7], NC_000004.12:g.75643297AT[8], NC_000004.12:g.75643297AT[9], NC_000004.12:g.75643297AT[11], NC_000004.12:g.75643297AT[12], NC_000004.12:g.75643296_75643316TA[13]CATATATATATATATATATATATAT[1], NC_000004.12:g.75643296_75643316TA[13]GATATATATATATATATATATAT[1], NC_000004.12:g.75643297AT[13], NC_000004.12:g.75643297AT[14], NC_000004.12:g.75643297AT[15], NC_000004.12:g.75643297AT[16], NC_000004.12:g.75643296_75643316TA[17]GATATATATATATATATATATATATATATATATATAT[1], NC_000004.12:g.75643297AT[17], NC_000004.12:g.75643297AT[18], NC_000004.12:g.75643297AT[19], NC_000004.12:g.75643297AT[20], NC_000004.12:g.75643296_75643316TA[21]AATATATATATATATATATATATATATAT[1], NC_000004.12:g.75643297AT[21], NC_000004.12:g.75643297AT[22], NC_000004.12:g.75643297AT[23], NC_000004.12:g.75643296_75643316TA[24]AATATATATATATATATATATATATATAT[1], NC_000004.12:g.75643297AT[24], NC_000004.12:g.75643297AT[25], NC_000004.12:g.75643297AT[26], NC_000004.12:g.75643297AT[27], NC_000004.12:g.75643296_75643316TA[28]GATATATATATATATATATATATAT[1], NC_000004.12:g.75643297AT[28], NC_000004.12:g.75643297AT[29], NC_000004.12:g.75643297AT[30], NC_000004.12:g.75643297AT[31], NC_000004.12:g.75643297AT[32], NC_000004.12:g.75643296_75643316TA[33]AATATATATATATATATATATATAT[1], NC_000004.12:g.75643297AT[33], NC_000004.12:g.75643297AT[34], NC_000004.11:g.76568481AT[4], NC_000004.11:g.76568481AT[5], NC_000004.11:g.76568481AT[6], NC_000004.11:g.76568481AT[7], NC_000004.11:g.76568481AT[8], NC_000004.11:g.76568481AT[9], NC_000004.11:g.76568481AT[11], NC_000004.11:g.76568481AT[12], NC_000004.11:g.76568480_76568500TA[13]CATATATATATATATATATATATAT[1], NC_000004.11:g.76568480_76568500TA[13]GATATATATATATATATATATAT[1], NC_000004.11:g.76568481AT[13], NC_000004.11:g.76568481AT[14], NC_000004.11:g.76568481AT[15], NC_000004.11:g.76568481AT[16], NC_000004.11:g.76568480_76568500TA[17]GATATATATATATATATATATATATATATATATATAT[1], NC_000004.11:g.76568481AT[17], NC_000004.11:g.76568481AT[18], NC_000004.11:g.76568481AT[19], NC_000004.11:g.76568481AT[20], NC_000004.11:g.76568480_76568500TA[21]AATATATATATATATATATATATATATAT[1], NC_000004.11:g.76568481AT[21], NC_000004.11:g.76568481AT[22], NC_000004.11:g.76568481AT[23], NC_000004.11:g.76568480_76568500TA[24]AATATATATATATATATATATATATATAT[1], NC_000004.11:g.76568481AT[24], NC_000004.11:g.76568481AT[25], NC_000004.11:g.76568481AT[26], NC_000004.11:g.76568481AT[27], NC_000004.11:g.76568480_76568500TA[28]GATATATATATATATATATATATAT[1], NC_000004.11:g.76568481AT[28], NC_000004.11:g.76568481AT[29], NC_000004.11:g.76568481AT[30], NC_000004.11:g.76568481AT[31], NC_000004.11:g.76568481AT[32], NC_000004.11:g.76568480_76568500TA[33]AATATATATATATATATATATATAT[1], NC_000004.11:g.76568481AT[33], NC_000004.11:g.76568481AT[34], NM_012297.5:c.*2115TA[4], NM_012297.5:c.*2115TA[5], NM_012297.5:c.*2115TA[6], NM_012297.5:c.*2115TA[7], NM_012297.5:c.*2115TA[8], NM_012297.5:c.*2115TA[9], NM_012297.5:c.*2115TA[11], NM_012297.5:c.*2115TA[12], NM_012297.5:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_012297.5:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_012297.5:c.*2115TA[13], NM_012297.5:c.*2115TA[14], NM_012297.5:c.*2115TA[15], NM_012297.5:c.*2115TA[16], NM_012297.5:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_012297.5:c.*2115TA[17], NM_012297.5:c.*2115TA[18], NM_012297.5:c.*2115TA[19], NM_012297.5:c.*2115TA[20], NM_012297.5:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.5:c.*2115TA[21], NM_012297.5:c.*2115TA[22], NM_012297.5:c.*2115TA[23], NM_012297.5:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.5:c.*2115TA[24], NM_012297.5:c.*2115TA[25], NM_012297.5:c.*2115TA[26], NM_012297.5:c.*2115TA[27], NM_012297.5:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.5:c.*2115TA[28], NM_012297.5:c.*2115TA[29], NM_012297.5:c.*2115TA[30], NM_012297.5:c.*2115TA[31], NM_012297.5:c.*2115TA[32], NM_012297.5:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.5:c.*2115TA[33], NM_012297.5:c.*2115TA[34], NM_012297.4:c.*2115TA[4], NM_012297.4:c.*2115TA[5], NM_012297.4:c.*2115TA[6], NM_012297.4:c.*2115TA[7], NM_012297.4:c.*2115TA[8], NM_012297.4:c.*2115TA[9], NM_012297.4:c.*2115TA[11], NM_012297.4:c.*2115TA[12], NM_012297.4:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_012297.4:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_012297.4:c.*2115TA[13], NM_012297.4:c.*2115TA[14], NM_012297.4:c.*2115TA[15], NM_012297.4:c.*2115TA[16], NM_012297.4:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_012297.4:c.*2115TA[17], NM_012297.4:c.*2115TA[18], NM_012297.4:c.*2115TA[19], NM_012297.4:c.*2115TA[20], NM_012297.4:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.4:c.*2115TA[21], NM_012297.4:c.*2115TA[22], NM_012297.4:c.*2115TA[23], NM_012297.4:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.4:c.*2115TA[24], NM_012297.4:c.*2115TA[25], NM_012297.4:c.*2115TA[26], NM_012297.4:c.*2115TA[27], NM_012297.4:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.4:c.*2115TA[28], NM_012297.4:c.*2115TA[29], NM_012297.4:c.*2115TA[30], NM_012297.4:c.*2115TA[31], NM_012297.4:c.*2115TA[32], NM_012297.4:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_012297.4:c.*2115TA[33], NM_012297.4:c.*2115TA[34], NM_203505.3:c.*2115TA[4], NM_203505.3:c.*2115TA[5], NM_203505.3:c.*2115TA[6], NM_203505.3:c.*2115TA[7], NM_203505.3:c.*2115TA[8], NM_203505.3:c.*2115TA[9], NM_203505.3:c.*2115TA[11], NM_203505.3:c.*2115TA[12], NM_203505.3:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_203505.3:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_203505.3:c.*2115TA[13], NM_203505.3:c.*2115TA[14], NM_203505.3:c.*2115TA[15], NM_203505.3:c.*2115TA[16], NM_203505.3:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_203505.3:c.*2115TA[17], NM_203505.3:c.*2115TA[18], NM_203505.3:c.*2115TA[19], NM_203505.3:c.*2115TA[20], NM_203505.3:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.3:c.*2115TA[21], NM_203505.3:c.*2115TA[22], NM_203505.3:c.*2115TA[23], NM_203505.3:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.3:c.*2115TA[24], NM_203505.3:c.*2115TA[25], NM_203505.3:c.*2115TA[26], NM_203505.3:c.*2115TA[27], NM_203505.3:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.3:c.*2115TA[28], NM_203505.3:c.*2115TA[29], NM_203505.3:c.*2115TA[30], NM_203505.3:c.*2115TA[31], NM_203505.3:c.*2115TA[32], NM_203505.3:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.3:c.*2115TA[33], NM_203505.3:c.*2115TA[34], NM_203505.2:c.*2115TA[4], NM_203505.2:c.*2115TA[5], NM_203505.2:c.*2115TA[6], NM_203505.2:c.*2115TA[7], NM_203505.2:c.*2115TA[8], NM_203505.2:c.*2115TA[9], NM_203505.2:c.*2115TA[11], NM_203505.2:c.*2115TA[12], NM_203505.2:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_203505.2:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_203505.2:c.*2115TA[13], NM_203505.2:c.*2115TA[14], NM_203505.2:c.*2115TA[15], NM_203505.2:c.*2115TA[16], NM_203505.2:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_203505.2:c.*2115TA[17], NM_203505.2:c.*2115TA[18], NM_203505.2:c.*2115TA[19], NM_203505.2:c.*2115TA[20], NM_203505.2:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.2:c.*2115TA[21], NM_203505.2:c.*2115TA[22], NM_203505.2:c.*2115TA[23], NM_203505.2:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.2:c.*2115TA[24], NM_203505.2:c.*2115TA[25], NM_203505.2:c.*2115TA[26], NM_203505.2:c.*2115TA[27], NM_203505.2:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.2:c.*2115TA[28], NM_203505.2:c.*2115TA[29], NM_203505.2:c.*2115TA[30], NM_203505.2:c.*2115TA[31], NM_203505.2:c.*2115TA[32], NM_203505.2:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203505.2:c.*2115TA[33], NM_203505.2:c.*2115TA[34], NM_203504.3:c.*2115TA[4], NM_203504.3:c.*2115TA[5], NM_203504.3:c.*2115TA[6], NM_203504.3:c.*2115TA[7], NM_203504.3:c.*2115TA[8], NM_203504.3:c.*2115TA[9], NM_203504.3:c.*2115TA[11], NM_203504.3:c.*2115TA[12], NM_203504.3:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_203504.3:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_203504.3:c.*2115TA[13], NM_203504.3:c.*2115TA[14], NM_203504.3:c.*2115TA[15], NM_203504.3:c.*2115TA[16], NM_203504.3:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_203504.3:c.*2115TA[17], NM_203504.3:c.*2115TA[18], NM_203504.3:c.*2115TA[19], NM_203504.3:c.*2115TA[20], NM_203504.3:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.3:c.*2115TA[21], NM_203504.3:c.*2115TA[22], NM_203504.3:c.*2115TA[23], NM_203504.3:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.3:c.*2115TA[24], NM_203504.3:c.*2115TA[25], NM_203504.3:c.*2115TA[26], NM_203504.3:c.*2115TA[27], NM_203504.3:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.3:c.*2115TA[28], NM_203504.3:c.*2115TA[29], NM_203504.3:c.*2115TA[30], NM_203504.3:c.*2115TA[31], NM_203504.3:c.*2115TA[32], NM_203504.3:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.3:c.*2115TA[33], NM_203504.3:c.*2115TA[34], NM_203504.2:c.*2115TA[4], NM_203504.2:c.*2115TA[5], NM_203504.2:c.*2115TA[6], NM_203504.2:c.*2115TA[7], NM_203504.2:c.*2115TA[8], NM_203504.2:c.*2115TA[9], NM_203504.2:c.*2115TA[11], NM_203504.2:c.*2115TA[12], NM_203504.2:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_203504.2:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_203504.2:c.*2115TA[13], NM_203504.2:c.*2115TA[14], NM_203504.2:c.*2115TA[15], NM_203504.2:c.*2115TA[16], NM_203504.2:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_203504.2:c.*2115TA[17], NM_203504.2:c.*2115TA[18], NM_203504.2:c.*2115TA[19], NM_203504.2:c.*2115TA[20], NM_203504.2:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.2:c.*2115TA[21], NM_203504.2:c.*2115TA[22], NM_203504.2:c.*2115TA[23], NM_203504.2:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.2:c.*2115TA[24], NM_203504.2:c.*2115TA[25], NM_203504.2:c.*2115TA[26], NM_203504.2:c.*2115TA[27], NM_203504.2:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.2:c.*2115TA[28], NM_203504.2:c.*2115TA[29], NM_203504.2:c.*2115TA[30], NM_203504.2:c.*2115TA[31], NM_203504.2:c.*2115TA[32], NM_203504.2:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_203504.2:c.*2115TA[33], NM_203504.2:c.*2115TA[34], XM_047416465.1:c.*2115TA[4], XM_047416465.1:c.*2115TA[5], XM_047416465.1:c.*2115TA[6], XM_047416465.1:c.*2115TA[7], XM_047416465.1:c.*2115TA[8], XM_047416465.1:c.*2115TA[9], XM_047416465.1:c.*2115TA[11], XM_047416465.1:c.*2115TA[12], XM_047416465.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], XM_047416465.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], XM_047416465.1:c.*2115TA[13], XM_047416465.1:c.*2115TA[14], XM_047416465.1:c.*2115TA[15], XM_047416465.1:c.*2115TA[16], XM_047416465.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], XM_047416465.1:c.*2115TA[17], XM_047416465.1:c.*2115TA[18], XM_047416465.1:c.*2115TA[19], XM_047416465.1:c.*2115TA[20], XM_047416465.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], XM_047416465.1:c.*2115TA[21], XM_047416465.1:c.*2115TA[22], XM_047416465.1:c.*2115TA[23], XM_047416465.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], XM_047416465.1:c.*2115TA[24], XM_047416465.1:c.*2115TA[25], XM_047416465.1:c.*2115TA[26], XM_047416465.1:c.*2115TA[27], XM_047416465.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], XM_047416465.1:c.*2115TA[28], XM_047416465.1:c.*2115TA[29], XM_047416465.1:c.*2115TA[30], XM_047416465.1:c.*2115TA[31], XM_047416465.1:c.*2115TA[32], XM_047416465.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], XM_047416465.1:c.*2115TA[33], XM_047416465.1:c.*2115TA[34], XM_047416466.1:c.*2115TA[4], XM_047416466.1:c.*2115TA[5], XM_047416466.1:c.*2115TA[6], XM_047416466.1:c.*2115TA[7], XM_047416466.1:c.*2115TA[8], XM_047416466.1:c.*2115TA[9], XM_047416466.1:c.*2115TA[11], XM_047416466.1:c.*2115TA[12], XM_047416466.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], XM_047416466.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], XM_047416466.1:c.*2115TA[13], XM_047416466.1:c.*2115TA[14], XM_047416466.1:c.*2115TA[15], XM_047416466.1:c.*2115TA[16], XM_047416466.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], XM_047416466.1:c.*2115TA[17], XM_047416466.1:c.*2115TA[18], XM_047416466.1:c.*2115TA[19], XM_047416466.1:c.*2115TA[20], XM_047416466.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], XM_047416466.1:c.*2115TA[21], XM_047416466.1:c.*2115TA[22], XM_047416466.1:c.*2115TA[23], XM_047416466.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], XM_047416466.1:c.*2115TA[24], XM_047416466.1:c.*2115TA[25], XM_047416466.1:c.*2115TA[26], XM_047416466.1:c.*2115TA[27], XM_047416466.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], XM_047416466.1:c.*2115TA[28], XM_047416466.1:c.*2115TA[29], XM_047416466.1:c.*2115TA[30], XM_047416466.1:c.*2115TA[31], XM_047416466.1:c.*2115TA[32], XM_047416466.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], XM_047416466.1:c.*2115TA[33], XM_047416466.1:c.*2115TA[34], NM_001400006.1:c.*2115TA[4], NM_001400006.1:c.*2115TA[5], NM_001400006.1:c.*2115TA[6], NM_001400006.1:c.*2115TA[7], NM_001400006.1:c.*2115TA[8], NM_001400006.1:c.*2115TA[9], NM_001400006.1:c.*2115TA[11], NM_001400006.1:c.*2115TA[12], NM_001400006.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400006.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400006.1:c.*2115TA[13], NM_001400006.1:c.*2115TA[14], NM_001400006.1:c.*2115TA[15], NM_001400006.1:c.*2115TA[16], NM_001400006.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400006.1:c.*2115TA[17], NM_001400006.1:c.*2115TA[18], NM_001400006.1:c.*2115TA[19], NM_001400006.1:c.*2115TA[20], NM_001400006.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400006.1:c.*2115TA[21], NM_001400006.1:c.*2115TA[22], NM_001400006.1:c.*2115TA[23], NM_001400006.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400006.1:c.*2115TA[24], NM_001400006.1:c.*2115TA[25], NM_001400006.1:c.*2115TA[26], NM_001400006.1:c.*2115TA[27], NM_001400006.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400006.1:c.*2115TA[28], NM_001400006.1:c.*2115TA[29], NM_001400006.1:c.*2115TA[30], NM_001400006.1:c.*2115TA[31], NM_001400006.1:c.*2115TA[32], NM_001400006.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400006.1:c.*2115TA[33], NM_001400006.1:c.*2115TA[34], NM_001400013.1:c.*2115TA[4], NM_001400013.1:c.*2115TA[5], NM_001400013.1:c.*2115TA[6], NM_001400013.1:c.*2115TA[7], NM_001400013.1:c.*2115TA[8], NM_001400013.1:c.*2115TA[9], NM_001400013.1:c.*2115TA[11], NM_001400013.1:c.*2115TA[12], NM_001400013.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400013.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400013.1:c.*2115TA[13], NM_001400013.1:c.*2115TA[14], NM_001400013.1:c.*2115TA[15], NM_001400013.1:c.*2115TA[16], NM_001400013.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400013.1:c.*2115TA[17], NM_001400013.1:c.*2115TA[18], NM_001400013.1:c.*2115TA[19], NM_001400013.1:c.*2115TA[20], NM_001400013.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400013.1:c.*2115TA[21], NM_001400013.1:c.*2115TA[22], NM_001400013.1:c.*2115TA[23], NM_001400013.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400013.1:c.*2115TA[24], NM_001400013.1:c.*2115TA[25], NM_001400013.1:c.*2115TA[26], NM_001400013.1:c.*2115TA[27], NM_001400013.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400013.1:c.*2115TA[28], NM_001400013.1:c.*2115TA[29], NM_001400013.1:c.*2115TA[30], NM_001400013.1:c.*2115TA[31], NM_001400013.1:c.*2115TA[32], NM_001400013.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400013.1:c.*2115TA[33], NM_001400013.1:c.*2115TA[34], NM_001400007.1:c.*2115TA[4], NM_001400007.1:c.*2115TA[5], NM_001400007.1:c.*2115TA[6], NM_001400007.1:c.*2115TA[7], NM_001400007.1:c.*2115TA[8], NM_001400007.1:c.*2115TA[9], NM_001400007.1:c.*2115TA[11], NM_001400007.1:c.*2115TA[12], NM_001400007.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400007.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400007.1:c.*2115TA[13], NM_001400007.1:c.*2115TA[14], NM_001400007.1:c.*2115TA[15], NM_001400007.1:c.*2115TA[16], NM_001400007.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400007.1:c.*2115TA[17], NM_001400007.1:c.*2115TA[18], NM_001400007.1:c.*2115TA[19], NM_001400007.1:c.*2115TA[20], NM_001400007.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400007.1:c.*2115TA[21], NM_001400007.1:c.*2115TA[22], NM_001400007.1:c.*2115TA[23], NM_001400007.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400007.1:c.*2115TA[24], NM_001400007.1:c.*2115TA[25], NM_001400007.1:c.*2115TA[26], NM_001400007.1:c.*2115TA[27], NM_001400007.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400007.1:c.*2115TA[28], NM_001400007.1:c.*2115TA[29], NM_001400007.1:c.*2115TA[30], NM_001400007.1:c.*2115TA[31], NM_001400007.1:c.*2115TA[32], NM_001400007.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400007.1:c.*2115TA[33], NM_001400007.1:c.*2115TA[34], NM_001400005.1:c.*2115TA[4], NM_001400005.1:c.*2115TA[5], NM_001400005.1:c.*2115TA[6], NM_001400005.1:c.*2115TA[7], NM_001400005.1:c.*2115TA[8], NM_001400005.1:c.*2115TA[9], NM_001400005.1:c.*2115TA[11], NM_001400005.1:c.*2115TA[12], NM_001400005.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400005.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400005.1:c.*2115TA[13], NM_001400005.1:c.*2115TA[14], NM_001400005.1:c.*2115TA[15], NM_001400005.1:c.*2115TA[16], NM_001400005.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400005.1:c.*2115TA[17], NM_001400005.1:c.*2115TA[18], NM_001400005.1:c.*2115TA[19], NM_001400005.1:c.*2115TA[20], NM_001400005.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400005.1:c.*2115TA[21], NM_001400005.1:c.*2115TA[22], NM_001400005.1:c.*2115TA[23], NM_001400005.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400005.1:c.*2115TA[24], NM_001400005.1:c.*2115TA[25], NM_001400005.1:c.*2115TA[26], NM_001400005.1:c.*2115TA[27], NM_001400005.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400005.1:c.*2115TA[28], NM_001400005.1:c.*2115TA[29], NM_001400005.1:c.*2115TA[30], NM_001400005.1:c.*2115TA[31], NM_001400005.1:c.*2115TA[32], NM_001400005.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400005.1:c.*2115TA[33], NM_001400005.1:c.*2115TA[34], NM_001400011.1:c.*2115TA[4], NM_001400011.1:c.*2115TA[5], NM_001400011.1:c.*2115TA[6], NM_001400011.1:c.*2115TA[7], NM_001400011.1:c.*2115TA[8], NM_001400011.1:c.*2115TA[9], NM_001400011.1:c.*2115TA[11], NM_001400011.1:c.*2115TA[12], NM_001400011.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400011.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400011.1:c.*2115TA[13], NM_001400011.1:c.*2115TA[14], NM_001400011.1:c.*2115TA[15], NM_001400011.1:c.*2115TA[16], NM_001400011.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400011.1:c.*2115TA[17], NM_001400011.1:c.*2115TA[18], NM_001400011.1:c.*2115TA[19], NM_001400011.1:c.*2115TA[20], NM_001400011.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400011.1:c.*2115TA[21], NM_001400011.1:c.*2115TA[22], NM_001400011.1:c.*2115TA[23], NM_001400011.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400011.1:c.*2115TA[24], NM_001400011.1:c.*2115TA[25], NM_001400011.1:c.*2115TA[26], NM_001400011.1:c.*2115TA[27], NM_001400011.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400011.1:c.*2115TA[28], NM_001400011.1:c.*2115TA[29], NM_001400011.1:c.*2115TA[30], NM_001400011.1:c.*2115TA[31], NM_001400011.1:c.*2115TA[32], NM_001400011.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400011.1:c.*2115TA[33], NM_001400011.1:c.*2115TA[34], NM_001400012.1:c.*2115TA[4], NM_001400012.1:c.*2115TA[5], NM_001400012.1:c.*2115TA[6], NM_001400012.1:c.*2115TA[7], NM_001400012.1:c.*2115TA[8], NM_001400012.1:c.*2115TA[9], NM_001400012.1:c.*2115TA[11], NM_001400012.1:c.*2115TA[12], NM_001400012.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400012.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400012.1:c.*2115TA[13], NM_001400012.1:c.*2115TA[14], NM_001400012.1:c.*2115TA[15], NM_001400012.1:c.*2115TA[16], NM_001400012.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400012.1:c.*2115TA[17], NM_001400012.1:c.*2115TA[18], NM_001400012.1:c.*2115TA[19], NM_001400012.1:c.*2115TA[20], NM_001400012.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400012.1:c.*2115TA[21], NM_001400012.1:c.*2115TA[22], NM_001400012.1:c.*2115TA[23], NM_001400012.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400012.1:c.*2115TA[24], NM_001400012.1:c.*2115TA[25], NM_001400012.1:c.*2115TA[26], NM_001400012.1:c.*2115TA[27], NM_001400012.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400012.1:c.*2115TA[28], NM_001400012.1:c.*2115TA[29], NM_001400012.1:c.*2115TA[30], NM_001400012.1:c.*2115TA[31], NM_001400012.1:c.*2115TA[32], NM_001400012.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400012.1:c.*2115TA[33], NM_001400012.1:c.*2115TA[34], NM_001400014.1:c.*2115TA[4], NM_001400014.1:c.*2115TA[5], NM_001400014.1:c.*2115TA[6], NM_001400014.1:c.*2115TA[7], NM_001400014.1:c.*2115TA[8], NM_001400014.1:c.*2115TA[9], NM_001400014.1:c.*2115TA[11], NM_001400014.1:c.*2115TA[12], NM_001400014.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400014.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400014.1:c.*2115TA[13], NM_001400014.1:c.*2115TA[14], NM_001400014.1:c.*2115TA[15], NM_001400014.1:c.*2115TA[16], NM_001400014.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400014.1:c.*2115TA[17], NM_001400014.1:c.*2115TA[18], NM_001400014.1:c.*2115TA[19], NM_001400014.1:c.*2115TA[20], NM_001400014.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400014.1:c.*2115TA[21], NM_001400014.1:c.*2115TA[22], NM_001400014.1:c.*2115TA[23], NM_001400014.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400014.1:c.*2115TA[24], NM_001400014.1:c.*2115TA[25], NM_001400014.1:c.*2115TA[26], NM_001400014.1:c.*2115TA[27], NM_001400014.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400014.1:c.*2115TA[28], NM_001400014.1:c.*2115TA[29], NM_001400014.1:c.*2115TA[30], NM_001400014.1:c.*2115TA[31], NM_001400014.1:c.*2115TA[32], NM_001400014.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400014.1:c.*2115TA[33], NM_001400014.1:c.*2115TA[34], NM_001400016.1:c.*2115TA[4], NM_001400016.1:c.*2115TA[5], NM_001400016.1:c.*2115TA[6], NM_001400016.1:c.*2115TA[7], NM_001400016.1:c.*2115TA[8], NM_001400016.1:c.*2115TA[9], NM_001400016.1:c.*2115TA[11], NM_001400016.1:c.*2115TA[12], NM_001400016.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400016.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400016.1:c.*2115TA[13], NM_001400016.1:c.*2115TA[14], NM_001400016.1:c.*2115TA[15], NM_001400016.1:c.*2115TA[16], NM_001400016.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400016.1:c.*2115TA[17], NM_001400016.1:c.*2115TA[18], NM_001400016.1:c.*2115TA[19], NM_001400016.1:c.*2115TA[20], NM_001400016.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400016.1:c.*2115TA[21], NM_001400016.1:c.*2115TA[22], NM_001400016.1:c.*2115TA[23], NM_001400016.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400016.1:c.*2115TA[24], NM_001400016.1:c.*2115TA[25], NM_001400016.1:c.*2115TA[26], NM_001400016.1:c.*2115TA[27], NM_001400016.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400016.1:c.*2115TA[28], NM_001400016.1:c.*2115TA[29], NM_001400016.1:c.*2115TA[30], NM_001400016.1:c.*2115TA[31], NM_001400016.1:c.*2115TA[32], NM_001400016.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400016.1:c.*2115TA[33], NM_001400016.1:c.*2115TA[34], NM_001400004.1:c.*2115TA[4], NM_001400004.1:c.*2115TA[5], NM_001400004.1:c.*2115TA[6], NM_001400004.1:c.*2115TA[7], NM_001400004.1:c.*2115TA[8], NM_001400004.1:c.*2115TA[9], NM_001400004.1:c.*2115TA[11], NM_001400004.1:c.*2115TA[12], NM_001400004.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400004.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400004.1:c.*2115TA[13], NM_001400004.1:c.*2115TA[14], NM_001400004.1:c.*2115TA[15], NM_001400004.1:c.*2115TA[16], NM_001400004.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400004.1:c.*2115TA[17], NM_001400004.1:c.*2115TA[18], NM_001400004.1:c.*2115TA[19], NM_001400004.1:c.*2115TA[20], NM_001400004.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400004.1:c.*2115TA[21], NM_001400004.1:c.*2115TA[22], NM_001400004.1:c.*2115TA[23], NM_001400004.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400004.1:c.*2115TA[24], NM_001400004.1:c.*2115TA[25], NM_001400004.1:c.*2115TA[26], NM_001400004.1:c.*2115TA[27], NM_001400004.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400004.1:c.*2115TA[28], NM_001400004.1:c.*2115TA[29], NM_001400004.1:c.*2115TA[30], NM_001400004.1:c.*2115TA[31], NM_001400004.1:c.*2115TA[32], NM_001400004.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400004.1:c.*2115TA[33], NM_001400004.1:c.*2115TA[34], NM_001400008.1:c.*2115TA[4], NM_001400008.1:c.*2115TA[5], NM_001400008.1:c.*2115TA[6], NM_001400008.1:c.*2115TA[7], NM_001400008.1:c.*2115TA[8], NM_001400008.1:c.*2115TA[9], NM_001400008.1:c.*2115TA[11], NM_001400008.1:c.*2115TA[12], NM_001400008.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400008.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400008.1:c.*2115TA[13], NM_001400008.1:c.*2115TA[14], NM_001400008.1:c.*2115TA[15], NM_001400008.1:c.*2115TA[16], NM_001400008.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400008.1:c.*2115TA[17], NM_001400008.1:c.*2115TA[18], NM_001400008.1:c.*2115TA[19], NM_001400008.1:c.*2115TA[20], NM_001400008.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400008.1:c.*2115TA[21], NM_001400008.1:c.*2115TA[22], NM_001400008.1:c.*2115TA[23], NM_001400008.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400008.1:c.*2115TA[24], NM_001400008.1:c.*2115TA[25], NM_001400008.1:c.*2115TA[26], NM_001400008.1:c.*2115TA[27], NM_001400008.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400008.1:c.*2115TA[28], NM_001400008.1:c.*2115TA[29], NM_001400008.1:c.*2115TA[30], NM_001400008.1:c.*2115TA[31], NM_001400008.1:c.*2115TA[32], NM_001400008.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400008.1:c.*2115TA[33], NM_001400008.1:c.*2115TA[34], NM_001400020.1:c.*2115TA[4], NM_001400020.1:c.*2115TA[5], NM_001400020.1:c.*2115TA[6], NM_001400020.1:c.*2115TA[7], NM_001400020.1:c.*2115TA[8], NM_001400020.1:c.*2115TA[9], NM_001400020.1:c.*2115TA[11], NM_001400020.1:c.*2115TA[12], NM_001400020.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400020.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400020.1:c.*2115TA[13], NM_001400020.1:c.*2115TA[14], NM_001400020.1:c.*2115TA[15], NM_001400020.1:c.*2115TA[16], NM_001400020.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400020.1:c.*2115TA[17], NM_001400020.1:c.*2115TA[18], NM_001400020.1:c.*2115TA[19], NM_001400020.1:c.*2115TA[20], NM_001400020.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400020.1:c.*2115TA[21], NM_001400020.1:c.*2115TA[22], NM_001400020.1:c.*2115TA[23], NM_001400020.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400020.1:c.*2115TA[24], NM_001400020.1:c.*2115TA[25], NM_001400020.1:c.*2115TA[26], NM_001400020.1:c.*2115TA[27], NM_001400020.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400020.1:c.*2115TA[28], NM_001400020.1:c.*2115TA[29], NM_001400020.1:c.*2115TA[30], NM_001400020.1:c.*2115TA[31], NM_001400020.1:c.*2115TA[32], NM_001400020.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400020.1:c.*2115TA[33], NM_001400020.1:c.*2115TA[34], NM_001400021.1:c.*2115TA[4], NM_001400021.1:c.*2115TA[5], NM_001400021.1:c.*2115TA[6], NM_001400021.1:c.*2115TA[7], NM_001400021.1:c.*2115TA[8], NM_001400021.1:c.*2115TA[9], NM_001400021.1:c.*2115TA[11], NM_001400021.1:c.*2115TA[12], NM_001400021.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400021.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400021.1:c.*2115TA[13], NM_001400021.1:c.*2115TA[14], NM_001400021.1:c.*2115TA[15], NM_001400021.1:c.*2115TA[16], NM_001400021.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400021.1:c.*2115TA[17], NM_001400021.1:c.*2115TA[18], NM_001400021.1:c.*2115TA[19], NM_001400021.1:c.*2115TA[20], NM_001400021.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400021.1:c.*2115TA[21], NM_001400021.1:c.*2115TA[22], NM_001400021.1:c.*2115TA[23], NM_001400021.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400021.1:c.*2115TA[24], NM_001400021.1:c.*2115TA[25], NM_001400021.1:c.*2115TA[26], NM_001400021.1:c.*2115TA[27], NM_001400021.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400021.1:c.*2115TA[28], NM_001400021.1:c.*2115TA[29], NM_001400021.1:c.*2115TA[30], NM_001400021.1:c.*2115TA[31], NM_001400021.1:c.*2115TA[32], NM_001400021.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400021.1:c.*2115TA[33], NM_001400021.1:c.*2115TA[34], NM_001400010.1:c.*2115TA[4], NM_001400010.1:c.*2115TA[5], NM_001400010.1:c.*2115TA[6], NM_001400010.1:c.*2115TA[7], NM_001400010.1:c.*2115TA[8], NM_001400010.1:c.*2115TA[9], NM_001400010.1:c.*2115TA[11], NM_001400010.1:c.*2115TA[12], NM_001400010.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400010.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400010.1:c.*2115TA[13], NM_001400010.1:c.*2115TA[14], NM_001400010.1:c.*2115TA[15], NM_001400010.1:c.*2115TA[16], NM_001400010.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400010.1:c.*2115TA[17], NM_001400010.1:c.*2115TA[18], NM_001400010.1:c.*2115TA[19], NM_001400010.1:c.*2115TA[20], NM_001400010.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400010.1:c.*2115TA[21], NM_001400010.1:c.*2115TA[22], NM_001400010.1:c.*2115TA[23], NM_001400010.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400010.1:c.*2115TA[24], NM_001400010.1:c.*2115TA[25], NM_001400010.1:c.*2115TA[26], NM_001400010.1:c.*2115TA[27], NM_001400010.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400010.1:c.*2115TA[28], NM_001400010.1:c.*2115TA[29], NM_001400010.1:c.*2115TA[30], NM_001400010.1:c.*2115TA[31], NM_001400010.1:c.*2115TA[32], NM_001400010.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400010.1:c.*2115TA[33], NM_001400010.1:c.*2115TA[34], NM_001400017.1:c.*2115TA[4], NM_001400017.1:c.*2115TA[5], NM_001400017.1:c.*2115TA[6], NM_001400017.1:c.*2115TA[7], NM_001400017.1:c.*2115TA[8], NM_001400017.1:c.*2115TA[9], NM_001400017.1:c.*2115TA[11], NM_001400017.1:c.*2115TA[12], NM_001400017.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400017.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400017.1:c.*2115TA[13], NM_001400017.1:c.*2115TA[14], NM_001400017.1:c.*2115TA[15], NM_001400017.1:c.*2115TA[16], NM_001400017.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400017.1:c.*2115TA[17], NM_001400017.1:c.*2115TA[18], NM_001400017.1:c.*2115TA[19], NM_001400017.1:c.*2115TA[20], NM_001400017.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400017.1:c.*2115TA[21], NM_001400017.1:c.*2115TA[22], NM_001400017.1:c.*2115TA[23], NM_001400017.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400017.1:c.*2115TA[24], NM_001400017.1:c.*2115TA[25], NM_001400017.1:c.*2115TA[26], NM_001400017.1:c.*2115TA[27], NM_001400017.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400017.1:c.*2115TA[28], NM_001400017.1:c.*2115TA[29], NM_001400017.1:c.*2115TA[30], NM_001400017.1:c.*2115TA[31], NM_001400017.1:c.*2115TA[32], NM_001400017.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400017.1:c.*2115TA[33], NM_001400017.1:c.*2115TA[34], NM_001400018.1:c.*2115TA[4], NM_001400018.1:c.*2115TA[5], NM_001400018.1:c.*2115TA[6], NM_001400018.1:c.*2115TA[7], NM_001400018.1:c.*2115TA[8], NM_001400018.1:c.*2115TA[9], NM_001400018.1:c.*2115TA[11], NM_001400018.1:c.*2115TA[12], NM_001400018.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400018.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400018.1:c.*2115TA[13], NM_001400018.1:c.*2115TA[14], NM_001400018.1:c.*2115TA[15], NM_001400018.1:c.*2115TA[16], NM_001400018.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400018.1:c.*2115TA[17], NM_001400018.1:c.*2115TA[18], NM_001400018.1:c.*2115TA[19], NM_001400018.1:c.*2115TA[20], NM_001400018.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400018.1:c.*2115TA[21], NM_001400018.1:c.*2115TA[22], NM_001400018.1:c.*2115TA[23], NM_001400018.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400018.1:c.*2115TA[24], NM_001400018.1:c.*2115TA[25], NM_001400018.1:c.*2115TA[26], NM_001400018.1:c.*2115TA[27], NM_001400018.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400018.1:c.*2115TA[28], NM_001400018.1:c.*2115TA[29], NM_001400018.1:c.*2115TA[30], NM_001400018.1:c.*2115TA[31], NM_001400018.1:c.*2115TA[32], NM_001400018.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400018.1:c.*2115TA[33], NM_001400018.1:c.*2115TA[34], NM_001400019.1:c.*2115TA[4], NM_001400019.1:c.*2115TA[5], NM_001400019.1:c.*2115TA[6], NM_001400019.1:c.*2115TA[7], NM_001400019.1:c.*2115TA[8], NM_001400019.1:c.*2115TA[9], NM_001400019.1:c.*2115TA[11], NM_001400019.1:c.*2115TA[12], NM_001400019.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400019.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400019.1:c.*2115TA[13], NM_001400019.1:c.*2115TA[14], NM_001400019.1:c.*2115TA[15], NM_001400019.1:c.*2115TA[16], NM_001400019.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400019.1:c.*2115TA[17], NM_001400019.1:c.*2115TA[18], NM_001400019.1:c.*2115TA[19], NM_001400019.1:c.*2115TA[20], NM_001400019.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400019.1:c.*2115TA[21], NM_001400019.1:c.*2115TA[22], NM_001400019.1:c.*2115TA[23], NM_001400019.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400019.1:c.*2115TA[24], NM_001400019.1:c.*2115TA[25], NM_001400019.1:c.*2115TA[26], NM_001400019.1:c.*2115TA[27], NM_001400019.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400019.1:c.*2115TA[28], NM_001400019.1:c.*2115TA[29], NM_001400019.1:c.*2115TA[30], NM_001400019.1:c.*2115TA[31], NM_001400019.1:c.*2115TA[32], NM_001400019.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400019.1:c.*2115TA[33], NM_001400019.1:c.*2115TA[34], NM_001400022.1:c.*2115TA[4], NM_001400022.1:c.*2115TA[5], NM_001400022.1:c.*2115TA[6], NM_001400022.1:c.*2115TA[7], NM_001400022.1:c.*2115TA[8], NM_001400022.1:c.*2115TA[9], NM_001400022.1:c.*2115TA[11], NM_001400022.1:c.*2115TA[12], NM_001400022.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400022.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400022.1:c.*2115TA[13], NM_001400022.1:c.*2115TA[14], NM_001400022.1:c.*2115TA[15], NM_001400022.1:c.*2115TA[16], NM_001400022.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400022.1:c.*2115TA[17], NM_001400022.1:c.*2115TA[18], NM_001400022.1:c.*2115TA[19], NM_001400022.1:c.*2115TA[20], NM_001400022.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400022.1:c.*2115TA[21], NM_001400022.1:c.*2115TA[22], NM_001400022.1:c.*2115TA[23], NM_001400022.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400022.1:c.*2115TA[24], NM_001400022.1:c.*2115TA[25], NM_001400022.1:c.*2115TA[26], NM_001400022.1:c.*2115TA[27], NM_001400022.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400022.1:c.*2115TA[28], NM_001400022.1:c.*2115TA[29], NM_001400022.1:c.*2115TA[30], NM_001400022.1:c.*2115TA[31], NM_001400022.1:c.*2115TA[32], NM_001400022.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400022.1:c.*2115TA[33], NM_001400022.1:c.*2115TA[34], NM_001400015.1:c.*2115TA[4], NM_001400015.1:c.*2115TA[5], NM_001400015.1:c.*2115TA[6], NM_001400015.1:c.*2115TA[7], NM_001400015.1:c.*2115TA[8], NM_001400015.1:c.*2115TA[9], NM_001400015.1:c.*2115TA[11], NM_001400015.1:c.*2115TA[12], NM_001400015.1:c.*2114_*2134AT[12]GTATATATATATATATATATATATATA[1], NM_001400015.1:c.*2114_*2134AT[11]CTATATATATATATATATATATATATA[1], NM_001400015.1:c.*2115TA[13], NM_001400015.1:c.*2115TA[14], NM_001400015.1:c.*2115TA[15], NM_001400015.1:c.*2115TA[16], NM_001400015.1:c.*2114_*2134AT[18]CTATATATATATATATATATATATATATATATATA[1], NM_001400015.1:c.*2115TA[17], NM_001400015.1:c.*2115TA[18], NM_001400015.1:c.*2115TA[19], NM_001400015.1:c.*2115TA[20], NM_001400015.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NM_001400015.1:c.*2115TA[21], NM_001400015.1:c.*2115TA[22], NM_001400015.1:c.*2115TA[23], NM_001400015.1:c.*2114_*2134AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400015.1:c.*2115TA[24], NM_001400015.1:c.*2115TA[25], NM_001400015.1:c.*2115TA[26], NM_001400015.1:c.*2115TA[27], NM_001400015.1:c.*2114_*2134AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400015.1:c.*2115TA[28], NM_001400015.1:c.*2115TA[29], NM_001400015.1:c.*2115TA[30], NM_001400015.1:c.*2115TA[31], NM_001400015.1:c.*2115TA[32], NM_001400015.1:c.*2114_*2134AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NM_001400015.1:c.*2115TA[33], NM_001400015.1:c.*2115TA[34], NR_174378.1:n.3428TA[4], NR_174378.1:n.3428TA[5], NR_174378.1:n.3428TA[6], NR_174378.1:n.3428TA[7], NR_174378.1:n.3428TA[8], NR_174378.1:n.3428TA[9], NR_174378.1:n.3428TA[11], NR_174378.1:n.3428TA[12], NR_174378.1:n.3427_3447AT[12]GTATATATATATATATATATATATATA[1], NR_174378.1:n.3427_3447AT[11]CTATATATATATATATATATATATATA[1], NR_174378.1:n.3428TA[13], NR_174378.1:n.3428TA[14], NR_174378.1:n.3428TA[15], NR_174378.1:n.3428TA[16], NR_174378.1:n.3427_3447AT[18]CTATATATATATATATATATATATATATATATATA[1], NR_174378.1:n.3428TA[17], NR_174378.1:n.3428TA[18], NR_174378.1:n.3428TA[19], NR_174378.1:n.3428TA[20], NR_174378.1:n.3427_3447AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NR_174378.1:n.3428TA[21], NR_174378.1:n.3428TA[22], NR_174378.1:n.3428TA[23], NR_174378.1:n.3427_3447AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174378.1:n.3428TA[24], NR_174378.1:n.3428TA[25], NR_174378.1:n.3428TA[26], NR_174378.1:n.3428TA[27], NR_174378.1:n.3427_3447AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174378.1:n.3428TA[28], NR_174378.1:n.3428TA[29], NR_174378.1:n.3428TA[30], NR_174378.1:n.3428TA[31], NR_174378.1:n.3428TA[32], NR_174378.1:n.3427_3447AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174378.1:n.3428TA[33], NR_174378.1:n.3428TA[34], NR_174377.1:n.3405TA[4], NR_174377.1:n.3405TA[5], NR_174377.1:n.3405TA[6], NR_174377.1:n.3405TA[7], NR_174377.1:n.3405TA[8], NR_174377.1:n.3405TA[9], NR_174377.1:n.3405TA[11], NR_174377.1:n.3405TA[12], NR_174377.1:n.3404_3424AT[12]GTATATATATATATATATATATATATA[1], NR_174377.1:n.3404_3424AT[11]CTATATATATATATATATATATATATA[1], NR_174377.1:n.3405TA[13], NR_174377.1:n.3405TA[14], NR_174377.1:n.3405TA[15], NR_174377.1:n.3405TA[16], NR_174377.1:n.3404_3424AT[18]CTATATATATATATATATATATATATATATATATA[1], NR_174377.1:n.3405TA[17], NR_174377.1:n.3405TA[18], NR_174377.1:n.3405TA[19], NR_174377.1:n.3405TA[20], NR_174377.1:n.3404_3424AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NR_174377.1:n.3405TA[21], NR_174377.1:n.3405TA[22], NR_174377.1:n.3405TA[23], NR_174377.1:n.3404_3424AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174377.1:n.3405TA[24], NR_174377.1:n.3405TA[25], NR_174377.1:n.3405TA[26], NR_174377.1:n.3405TA[27], NR_174377.1:n.3404_3424AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174377.1:n.3405TA[28], NR_174377.1:n.3405TA[29], NR_174377.1:n.3405TA[30], NR_174377.1:n.3405TA[31], NR_174377.1:n.3405TA[32], NR_174377.1:n.3404_3424AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174377.1:n.3405TA[33], NR_174377.1:n.3405TA[34], NR_174376.1:n.3363TA[4], NR_174376.1:n.3363TA[5], NR_174376.1:n.3363TA[6], NR_174376.1:n.3363TA[7], NR_174376.1:n.3363TA[8], NR_174376.1:n.3363TA[9], NR_174376.1:n.3363TA[11], NR_174376.1:n.3363TA[12], NR_174376.1:n.3362_3382AT[12]GTATATATATATATATATATATATATA[1], NR_174376.1:n.3362_3382AT[11]CTATATATATATATATATATATATATA[1], NR_174376.1:n.3363TA[13], NR_174376.1:n.3363TA[14], NR_174376.1:n.3363TA[15], NR_174376.1:n.3363TA[16], NR_174376.1:n.3362_3382AT[18]CTATATATATATATATATATATATATATATATATA[1], NR_174376.1:n.3363TA[17], NR_174376.1:n.3363TA[18], NR_174376.1:n.3363TA[19], NR_174376.1:n.3363TA[20], NR_174376.1:n.3362_3382AT[14]TTATATATATATATATATATATATATATATATATATATATATA[1], NR_174376.1:n.3363TA[21], NR_174376.1:n.3363TA[22], NR_174376.1:n.3363TA[23], NR_174376.1:n.3362_3382AT[14]TTATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174376.1:n.3363TA[24], NR_174376.1:n.3363TA[25], NR_174376.1:n.3363TA[26], NR_174376.1:n.3363TA[27], NR_174376.1:n.3362_3382AT[12]CTATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174376.1:n.3363TA[28], NR_174376.1:n.3363TA[29], NR_174376.1:n.3363TA[30], NR_174376.1:n.3363TA[31], NR_174376.1:n.3363TA[32], NR_174376.1:n.3362_3382AT[12]TTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA[1], NR_174376.1:n.3363TA[33], NR_174376.1:n.3363TA[34]

          5.

          rs1491502527 [Homo sapiens]
            Variant type:
            SNV:
            Alleles:
            GG>-
            Chromosome:
            no mapping
            Canonical SPDI:

            6.

            rs1491492749 [Homo sapiens]
              Variant type:
              INS
              Alleles:
              ->G [Show Flanks]
              Chromosome:
              4:75726282 (GRCh38)
              4:76651467 (GRCh37)
              Canonical SPDI:
              NC_000004.12:75726282::G
              Gene:
              USO1 (Varview), G3BP2 (Varview)
              Functional Consequence:
              intron_variant,upstream_transcript_variant,2KB_upstream_variant
              Validated:
              by frequency,by alfa
              MAF:
              G=0./0 (ALFA)
              G=0.000004/1 (TOPMED)
              HGVS:

              7.

              rs1491491294 [Homo sapiens]
                Variant type:
                DEL
                Alleles:
                TA>- [Show Flanks]
                Chromosome:
                4:75671696 (GRCh38)
                4:76596880 (GRCh37)
                Canonical SPDI:
                NC_000004.12:75671695:TA:
                Gene:
                G3BP2 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                -=0.000071/1 (ALFA)
                -=0.000004/1 (TOPMED)
                -=0.000007/1 (GnomAD)
                HGVS:

                8.

                rs1491482854 has merged into rs34603185 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  AAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA [Show Flanks]
                  Chromosome:
                  4:75709431 (GRCh38)
                  4:76634615 (GRCh37)
                  Canonical SPDI:
                  NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75709419:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                  Gene:
                  G3BP2 (Varview)
                  Functional Consequence:
                  intron_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AAAAAAAAAAAAA=0./0 (ALFA)
                  HGVS:
                  NC_000004.12:g.75709431_75709442del, NC_000004.12:g.75709433_75709442del, NC_000004.12:g.75709434_75709442del, NC_000004.12:g.75709435_75709442del, NC_000004.12:g.75709436_75709442del, NC_000004.12:g.75709437_75709442del, NC_000004.12:g.75709438_75709442del, NC_000004.12:g.75709439_75709442del, NC_000004.12:g.75709440_75709442del, NC_000004.12:g.75709441_75709442del, NC_000004.12:g.75709442del, NC_000004.12:g.75709442dup, NC_000004.12:g.75709441_75709442dup, NC_000004.12:g.75709440_75709442dup, NC_000004.12:g.75709439_75709442dup, NC_000004.12:g.75709438_75709442dup, NC_000004.12:g.75709437_75709442dup, NC_000004.12:g.75709436_75709442dup, NC_000004.12:g.75709435_75709442dup, NC_000004.11:g.76634615_76634626del, NC_000004.11:g.76634617_76634626del, NC_000004.11:g.76634618_76634626del, NC_000004.11:g.76634619_76634626del, NC_000004.11:g.76634620_76634626del, NC_000004.11:g.76634621_76634626del, NC_000004.11:g.76634622_76634626del, NC_000004.11:g.76634623_76634626del, NC_000004.11:g.76634624_76634626del, NC_000004.11:g.76634625_76634626del, NC_000004.11:g.76634626del, NC_000004.11:g.76634626dup, NC_000004.11:g.76634625_76634626dup, NC_000004.11:g.76634624_76634626dup, NC_000004.11:g.76634623_76634626dup, NC_000004.11:g.76634622_76634626dup, NC_000004.11:g.76634621_76634626dup, NC_000004.11:g.76634620_76634626dup, NC_000004.11:g.76634619_76634626dup

                  9.

                  rs1491432909 [Homo sapiens]
                    Variant type:
                    INS
                    Alleles:
                    ->AAG,AG [Show Flanks]
                    Chromosome:
                    4:75726301 (GRCh38)
                    4:76651486 (GRCh37)
                    Canonical SPDI:
                    NC_000004.12:75726301::AAG,NC_000004.12:75726301::AG
                    Gene:
                    USO1 (Varview), G3BP2 (Varview)
                    Functional Consequence:
                    intron_variant,upstream_transcript_variant,2KB_upstream_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AG=0./0 (ALFA)
                    HGVS:

                    10.

                    rs1491427062 has merged into rs71203842 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      TTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                      Chromosome:
                      4:75674724 (GRCh38)
                      4:76599908 (GRCh37)
                      Canonical SPDI:
                      NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75674718:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                      Gene:
                      G3BP2 (Varview)
                      Functional Consequence:
                      upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      TTTTTT=0./0 (ALFA)
                      HGVS:
                      NC_000004.12:g.75674724_75674740del, NC_000004.12:g.75674725_75674740del, NC_000004.12:g.75674726_75674740del, NC_000004.12:g.75674727_75674740del, NC_000004.12:g.75674728_75674740del, NC_000004.12:g.75674729_75674740del, NC_000004.12:g.75674730_75674740del, NC_000004.12:g.75674731_75674740del, NC_000004.12:g.75674732_75674740del, NC_000004.12:g.75674733_75674740del, NC_000004.12:g.75674734_75674740del, NC_000004.12:g.75674735_75674740del, NC_000004.12:g.75674736_75674740del, NC_000004.12:g.75674737_75674740del, NC_000004.12:g.75674738_75674740del, NC_000004.12:g.75674739_75674740del, NC_000004.12:g.75674740del, NC_000004.12:g.75674740dup, NC_000004.12:g.75674739_75674740dup, NC_000004.12:g.75674738_75674740dup, NC_000004.12:g.75674737_75674740dup, NC_000004.12:g.75674736_75674740dup, NC_000004.12:g.75674735_75674740dup, NC_000004.12:g.75674734_75674740dup, NC_000004.12:g.75674733_75674740dup, NC_000004.12:g.75674730_75674740dup, NC_000004.11:g.76599908_76599924del, NC_000004.11:g.76599909_76599924del, NC_000004.11:g.76599910_76599924del, NC_000004.11:g.76599911_76599924del, NC_000004.11:g.76599912_76599924del, NC_000004.11:g.76599913_76599924del, NC_000004.11:g.76599914_76599924del, NC_000004.11:g.76599915_76599924del, NC_000004.11:g.76599916_76599924del, NC_000004.11:g.76599917_76599924del, NC_000004.11:g.76599918_76599924del, NC_000004.11:g.76599919_76599924del, NC_000004.11:g.76599920_76599924del, NC_000004.11:g.76599921_76599924del, NC_000004.11:g.76599922_76599924del, NC_000004.11:g.76599923_76599924del, NC_000004.11:g.76599924del, NC_000004.11:g.76599924dup, NC_000004.11:g.76599923_76599924dup, NC_000004.11:g.76599922_76599924dup, NC_000004.11:g.76599921_76599924dup, NC_000004.11:g.76599920_76599924dup, NC_000004.11:g.76599919_76599924dup, NC_000004.11:g.76599918_76599924dup, NC_000004.11:g.76599917_76599924dup, NC_000004.11:g.76599914_76599924dup

                      11.

                      rs1491425061 [Homo sapiens]
                        Variant type:
                        INS
                        Alleles:
                        ->A [Show Flanks]
                        Chromosome:
                        4:75715301 (GRCh38)
                        4:76640486 (GRCh37)
                        Canonical SPDI:
                        NC_000004.12:75715301::A
                        Gene:
                        G3BP2 (Varview)
                        Functional Consequence:
                        intron_variant,genic_upstream_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        A=0./0 (ALFA)
                        A=0.000004/1 (TOPMED)
                        HGVS:

                        12.

                        rs1491417044 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          ->CTT [Show Flanks]
                          Chromosome:
                          4:75718239 (GRCh38)
                          4:76643424 (GRCh37)
                          Canonical SPDI:
                          NC_000004.12:75718239:TT:TTCTT
                          Gene:
                          G3BP2 (Varview)
                          Functional Consequence:
                          intron_variant,genic_upstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          TTCTT=0./0 (ALFA)
                          TTC=0.000008/2 (TOPMED)
                          TTC=0.001266/2 (GnomAD)
                          HGVS:

                          13.

                          rs1491386564 has merged into rs34017434 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            TTTTTTTTTTTTTTT>-,TT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                            Chromosome:
                            4:75676346 (GRCh38)
                            4:76601530 (GRCh37)
                            Canonical SPDI:
                            NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:75676336:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                            Gene:
                            G3BP2 (Varview)
                            Functional Consequence:
                            intron_variant,genic_upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTTTTTTT=0./0 (ALFA)
                            -=0.088/339 (ALSPAC)
                            -=0.0947/351 (TWINSUK)
                            HGVS:
                            NC_000004.12:g.75676346_75676360del, NC_000004.12:g.75676348_75676360del, NC_000004.12:g.75676350_75676360del, NC_000004.12:g.75676352_75676360del, NC_000004.12:g.75676353_75676360del, NC_000004.12:g.75676354_75676360del, NC_000004.12:g.75676355_75676360del, NC_000004.12:g.75676356_75676360del, NC_000004.12:g.75676357_75676360del, NC_000004.12:g.75676358_75676360del, NC_000004.12:g.75676359_75676360del, NC_000004.12:g.75676360del, NC_000004.12:g.75676360dup, NC_000004.12:g.75676359_75676360dup, NC_000004.12:g.75676358_75676360dup, NC_000004.12:g.75676357_75676360dup, NC_000004.12:g.75676356_75676360dup, NC_000004.12:g.75676355_75676360dup, NC_000004.12:g.75676354_75676360dup, NC_000004.12:g.75676353_75676360dup, NC_000004.12:g.75676352_75676360dup, NC_000004.12:g.75676347_75676360dup, NC_000004.12:g.75676337_75676360dup, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.75676360_75676361insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601530_76601544del, NC_000004.11:g.76601532_76601544del, NC_000004.11:g.76601534_76601544del, NC_000004.11:g.76601536_76601544del, NC_000004.11:g.76601537_76601544del, NC_000004.11:g.76601538_76601544del, NC_000004.11:g.76601539_76601544del, NC_000004.11:g.76601540_76601544del, NC_000004.11:g.76601541_76601544del, NC_000004.11:g.76601542_76601544del, NC_000004.11:g.76601543_76601544del, NC_000004.11:g.76601544del, NC_000004.11:g.76601544dup, NC_000004.11:g.76601543_76601544dup, NC_000004.11:g.76601542_76601544dup, NC_000004.11:g.76601541_76601544dup, NC_000004.11:g.76601540_76601544dup, NC_000004.11:g.76601539_76601544dup, NC_000004.11:g.76601538_76601544dup, NC_000004.11:g.76601537_76601544dup, NC_000004.11:g.76601536_76601544dup, NC_000004.11:g.76601531_76601544dup, NC_000004.11:g.76601521_76601544dup, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.76601544_76601545insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

                            14.

                            rs1491353767 [Homo sapiens]
                              Variant type:
                              DEL
                              Alleles:
                              AG>- [Show Flanks]
                              Chromosome:
                              4:75726301 (GRCh38)
                              4:76651485 (GRCh37)
                              Canonical SPDI:
                              NC_000004.12:75726300:AG:
                              Gene:
                              USO1 (Varview), G3BP2 (Varview)
                              Functional Consequence:
                              intron_variant,upstream_transcript_variant,2KB_upstream_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              -=0./0 (ALFA)
                              -=0.000203/28 (GnomAD)
                              HGVS:

                              15.

                              rs1491322732 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                ->A [Show Flanks]
                                Chromosome:
                                4:75671696 (GRCh38)
                                4:76596881 (GRCh37)
                                Canonical SPDI:
                                NC_000004.12:75671696:A:AA
                                Gene:
                                G3BP2 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                AA=0.000142/2 (ALFA)
                                A=0.000049/13 (TOPMED)
                                A=0.000071/10 (GnomAD)
                                HGVS:

                                16.

                                rs1491292385 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  ->GAA [Show Flanks]
                                  Chromosome:
                                  4:75709420 (GRCh38)
                                  4:76634605 (GRCh37)
                                  Canonical SPDI:
                                  NC_000004.12:75709420:AA:AAGAA
                                  Gene:
                                  G3BP2 (Varview)
                                  Functional Consequence:
                                  intron_variant,genic_upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  AAGAA=0.00624/74 (ALFA)
                                  AAG=0.03836/971 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1491279138 [Homo sapiens]
                                    Variant type:
                                    INS
                                    Alleles:
                                    ->C [Show Flanks]
                                    Chromosome:
                                    4:75684794 (GRCh38)
                                    4:76609979 (GRCh37)
                                    Canonical SPDI:
                                    NC_000004.12:75684794::C
                                    Gene:
                                    G3BP2 (Varview)
                                    Functional Consequence:
                                    intron_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    C=0./0 (ALFA)
                                    HGVS:

                                    18.

                                    rs1491263562 has merged into rs35357713 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      AAAAAAAAA>-,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
                                      Chromosome:
                                      4:75707185 (GRCh38)
                                      4:76632369 (GRCh37)
                                      Canonical SPDI:
                                      NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:75707175:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA
                                      Gene:
                                      G3BP2 (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      AAAAAAAAAAAAAAA=0./0 (ALFA)
                                      A=0.4445/2226 (1000Genomes)
                                      HGVS:

                                      19.

                                      rs1491223136 has merged into rs11339894 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT [Show Flanks]
                                        Chromosome:
                                        4:75718246 (GRCh38)
                                        4:76643430 (GRCh37)
                                        Canonical SPDI:
                                        NC_000004.12:75718238:TTTTTTTTTTTT:TTTTTTT,NC_000004.12:75718238:TTTTTTTTTTTT:TTTTTTTT,NC_000004.12:75718238:TTTTTTTTTTTT:TTTTTTTTT,NC_000004.12:75718238:TTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:75718238:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:75718238:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:75718238:TTTTTTTTTTTT:TTTTTTTTTTTTTT
                                        Gene:
                                        G3BP2 (Varview)
                                        Functional Consequence:
                                        intron_variant,genic_upstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        TTTTTTTTTTTTT=0.00022/1 (ALFA)
                                        T=0.05089/853 (TOMMO)
                                        T=0.09465/474 (1000Genomes)
                                        T=0.11704/434 (TWINSUK)
                                        T=0.11936/460 (ALSPAC)
                                        T=0.12162/72 (NorthernSweden)
                                        T=0.125/5 (GENOME_DK)
                                        HGVS:

                                        20.

                                        rs1491211118 has merged into rs905580307 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          TTTTT>-,TTT,TTTT,TTTTTT,TTTTTTT [Show Flanks]
                                          Chromosome:
                                          4:75684800 (GRCh38)
                                          4:76609984 (GRCh37)
                                          Canonical SPDI:
                                          NC_000004.12:75684793:TTTTTTTTTTT:TTTTTT,NC_000004.12:75684793:TTTTTTTTTTT:TTTTTTTTT,NC_000004.12:75684793:TTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:75684793:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:75684793:TTTTTTTTTTT:TTTTTTTTTTTTT
                                          Gene:
                                          G3BP2 (Varview)
                                          Functional Consequence:
                                          intron_variant,genic_upstream_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          TTTTTTTTT=0./0 (ALFA)
                                          HGVS:

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