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1.

rs1491151970 [Homo sapiens]
    Variant type:
    DEL
    Alleles:
    TG>- [Show Flanks]
    Chromosome:
    6:65789525 (GRCh38)
    6:66499418 (GRCh37)
    Canonical SPDI:
    NC_000006.12:65789524:TG:
    Gene:
    SLC25A51P1 (Varview)
    Functional Consequence:
    downstream_transcript_variant,500B_downstream_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    -=0.000253/3 (ALFA)
    -=0.000706/78 (GnomAD)
    -=0.001874/12 (1000Genomes)
    HGVS:

    2.

    rs1491098989 has merged into rs35228595 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TTTT>-,T,TT,TTT,TTTTT,TTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTGTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTT,TTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTCTTTTTTTTTTTTTTTTTT,TTTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTT,TTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTT,TTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTATTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTT,TTTTTTTTCTTTTTTTTTTTTTTTTTT,TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTGTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
      Chromosome:
      6:65789522 (GRCh38)
      6:66499415 (GRCh37)
      Canonical SPDI:
      NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTT,NC_000006.12:65789510:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
      Gene:
      SLC25A51P1 (Varview)
      Functional Consequence:
      downstream_transcript_variant,500B_downstream_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TTTTTTTTTTTT=0./0 (ALFA)
      HGVS:
      NC_000006.12:g.65789522_65789525del, NC_000006.12:g.65789523_65789525del, NC_000006.12:g.65789524_65789525del, NC_000006.12:g.65789525del, NC_000006.12:g.65789525dup, NC_000006.12:g.65789511_65789525T[16]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTT[2]T[8], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTT[2]T[14], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTT[2]T[16], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTT[2]T[19], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTT[2]T[20], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTT[2]T[21], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTT[2]T[30], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789524_65789525dup, NC_000006.12:g.65789511_65789525T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]CTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GTTTTTTTT[2]T[20], NC_000006.12:g.65789511_65789525T[17]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789523_65789525dup, NC_000006.12:g.65789511_65789525T[18]ATTTTTTTGTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]ATTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]GTTTTTTT[2]T[17], NC_000006.12:g.65789511_65789525T[18]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]GTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789522_65789525dup, NC_000006.12:g.65789511_65789525T[19]CTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[19]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[19]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[19]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789521_65789525dup, NC_000006.12:g.65789517_65789525dup, NC_000006.12:g.65789516_65789525dup, NC_000006.12:g.65789511_65789525T[25]GTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[25]GTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[25]GTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[25]GTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[26]GTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[26]GTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[27]GTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789511_65789525T[27]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789511_65789525T[45]CTTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.65789511_65789525T[61]GTTTTTTTTTTTTTTTTT[1], NC_000006.12:g.65789525_65789526insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499415_66499418del, NC_000006.11:g.66499416_66499418del, NC_000006.11:g.66499417_66499418del, NC_000006.11:g.66499418del, NC_000006.11:g.66499418dup, NC_000006.11:g.66499404_66499418T[16]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTT[2]T[8], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTT[2]T[14], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTT[2]T[16], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTT[2]T[19], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTT[2]T[20], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTT[2]T[21], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTT[2]T[30], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499417_66499418dup, NC_000006.11:g.66499404_66499418T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]CTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GTTTTTTTT[2]T[20], NC_000006.11:g.66499404_66499418T[17]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499416_66499418dup, NC_000006.11:g.66499404_66499418T[18]ATTTTTTTGTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]ATTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]GTTTTTTT[2]T[17], NC_000006.11:g.66499404_66499418T[18]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]GTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499415_66499418dup, NC_000006.11:g.66499404_66499418T[19]CTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[19]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[19]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[19]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499414_66499418dup, NC_000006.11:g.66499410_66499418dup, NC_000006.11:g.66499409_66499418dup, NC_000006.11:g.66499404_66499418T[25]GTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[25]GTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[25]GTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[25]GTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[26]GTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[26]GTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[27]GTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499404_66499418T[27]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499404_66499418T[45]CTTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.66499404_66499418T[61]GTTTTTTTTTTTTTTTTT[1], NC_000006.11:g.66499418_66499419insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14709_14712del, NT_187555.1:g.14710_14712del, NT_187555.1:g.14711_14712del, NT_187555.1:g.14712del, NT_187555.1:g.14712dup, NT_187555.1:g.14698_14712T[16]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GGTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTT[2]T[8], NT_187555.1:g.14698_14712T[16]GTTTTTTTT[2]T[14], NT_187555.1:g.14698_14712T[16]GTTTTTTTT[2]T[16], NT_187555.1:g.14698_14712T[16]GTTTTTTTT[2]T[19], NT_187555.1:g.14698_14712T[16]GTTTTTTTT[2]T[20], NT_187555.1:g.14698_14712T[16]GTTTTTTTT[2]T[21], NT_187555.1:g.14698_14712T[16]GTTTTTTTT[2]T[30], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[16]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14711_14712dup, NT_187555.1:g.14698_14712T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]CTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GTTTTTTTT[2]T[20], NT_187555.1:g.14698_14712T[17]GTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[17]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14710_14712dup, NT_187555.1:g.14698_14712T[18]ATTTTTTTGTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]ATTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]ATTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]GGTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]GTTTTTTT[2]T[17], NT_187555.1:g.14698_14712T[18]GTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]GTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[18]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14709_14712dup, NT_187555.1:g.14698_14712T[19]CTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[19]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[19]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[19]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14708_14712dup, NT_187555.1:g.14704_14712dup, NT_187555.1:g.14703_14712dup, NT_187555.1:g.14698_14712T[25]GTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[25]GTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[25]GTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[25]GTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[26]GTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[26]GTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[27]GTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14698_14712T[27]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14698_14712T[45]CTTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187555.1:g.14698_14712T[61]GTTTTTTTTTTTTTTTTT[1], NT_187555.1:g.14712_14713insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

      3.

      rs1489904325 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>A [Show Flanks]
        Chromosome:
        6:65785898 (GRCh38)
        6:66495791 (GRCh37)
        Canonical SPDI:
        NC_000006.12:65785897:T:A
        Gene:
        SLC25A51P1 (Varview)
        Functional Consequence:
        2KB_upstream_variant,upstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0./0 (ALFA)
        A=0.000007/1 (GnomAD)
        A=0.000008/2 (TOPMED)
        T=0.5/1 (SGDP_PRJ)
        HGVS:

        4.

        rs1489747494 [Homo sapiens]
          Variant type:
          SNV:
          Alleles:
          ->C
          Chromosome:
          no mapping
          Canonical SPDI:

          5.

          rs1489400730 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            6:65787346 (GRCh38)
            6:66497239 (GRCh37)
            Canonical SPDI:
            NC_000006.12:65787345:A:G
            Gene:
            SLC25A51P1 (Varview)
            Functional Consequence:
            2KB_upstream_variant,upstream_transcript_variant
            Validated:
            by frequency,by alfa
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            HGVS:

            6.

            rs1489329264 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>A [Show Flanks]
              Chromosome:
              6:65786377 (GRCh38)
              6:66496270 (GRCh37)
              Canonical SPDI:
              NC_000006.12:65786376:C:A
              Gene:
              SLC25A51P1 (Varview)
              Functional Consequence:
              2KB_upstream_variant,upstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              A=0./0 (ALFA)
              A=0.000007/1 (GnomAD)
              A=0.000008/2 (TOPMED)
              HGVS:

              7.

              rs1489058212 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>C,G [Show Flanks]
                Chromosome:
                6:65788780 (GRCh38)
                6:66498673 (GRCh37)
                Canonical SPDI:
                NC_000006.12:65788779:A:C,NC_000006.12:65788779:A:G
                Gene:
                SLC25A51P1 (Varview)
                Functional Consequence:
                non_coding_transcript_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                G=0./0 (ALFA)
                A=0.5/1 (SGDP_PRJ)
                HGVS:

                8.

                rs1486665055 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>C [Show Flanks]
                  Chromosome:
                  6:65786648 (GRCh38)
                  6:66496541 (GRCh37)
                  Canonical SPDI:
                  NC_000006.12:65786647:T:C
                  Gene:
                  SLC25A51P1 (Varview)
                  Functional Consequence:
                  2KB_upstream_variant,upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0.000071/1 (ALFA)
                  C=0.000015/4 (TOPMED)
                  C=0.000021/3 (GnomAD)
                  HGVS:

                  9.

                  rs1486227343 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>A [Show Flanks]
                    Chromosome:
                    6:65789340 (GRCh38)
                    6:66499233 (GRCh37)
                    Canonical SPDI:
                    NC_000006.12:65789339:C:A
                    Gene:
                    SLC25A51P1 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    A=0./0 (ALFA)
                    HGVS:

                    10.

                    rs1486195131 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>G [Show Flanks]
                      Chromosome:
                      6:65788265 (GRCh38)
                      6:66498158 (GRCh37)
                      Canonical SPDI:
                      NC_000006.12:65788264:C:G
                      Gene:
                      SLC25A51P1 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      G=0.000071/1 (ALFA)
                      G=0.000008/2 (TOPMED)
                      HGVS:

                      11.

                      rs1485647245 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        6:65789886 (GRCh38)
                        6:66499779 (GRCh37)
                        Canonical SPDI:
                        NC_000006.12:65789885:C:T
                        Gene:
                        SLC25A51P1 (Varview)
                        Functional Consequence:
                        downstream_transcript_variant,500B_downstream_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000011/3 (TOPMED)
                        T=0.000014/2 (GnomAD)
                        HGVS:

                        12.

                        rs1485027198 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>A [Show Flanks]
                          Chromosome:
                          6:65789150 (GRCh38)
                          6:66499043 (GRCh37)
                          Canonical SPDI:
                          NC_000006.12:65789149:T:A
                          Gene:
                          SLC25A51P1 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000004/1 (TOPMED)
                          HGVS:

                          13.

                          rs1484705542 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            6:65788530 (GRCh38)
                            6:66498423 (GRCh37)
                            Canonical SPDI:
                            NC_000006.12:65788529:C:T
                            Gene:
                            SLC25A51P1 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000004/1 (TOPMED)
                            T=0.000014/2 (GnomAD)
                            HGVS:

                            14.

                            rs1484233655 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>G [Show Flanks]
                              Chromosome:
                              6:65787655 (GRCh38)
                              6:66497548 (GRCh37)
                              Canonical SPDI:
                              NC_000006.12:65787654:A:G
                              Gene:
                              SLC25A51P1 (Varview)
                              Functional Consequence:
                              2KB_upstream_variant,upstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000011/3 (TOPMED)
                              G=0.000342/1 (KOREAN)
                              HGVS:

                              15.

                              rs1484164088 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G,T [Show Flanks]
                                Chromosome:
                                6:65786712 (GRCh38)
                                6:66496605 (GRCh37)
                                Canonical SPDI:
                                NC_000006.12:65786711:A:G,NC_000006.12:65786711:A:T
                                Gene:
                                SLC25A51P1 (Varview)
                                Functional Consequence:
                                2KB_upstream_variant,upstream_transcript_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                T=0./0 (ALFA)
                                G=0.000015/2 (GnomAD)
                                HGVS:

                                16.

                                rs1484077987 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>A,T [Show Flanks]
                                  Chromosome:
                                  6:65787998 (GRCh38)
                                  6:66497891 (GRCh37)
                                  Canonical SPDI:
                                  NC_000006.12:65787997:G:A,NC_000006.12:65787997:G:T
                                  Gene:
                                  SLC25A51P1 (Varview)
                                  Functional Consequence:
                                  non_coding_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0.00007/1 (ALFA)
                                  HGVS:

                                  17.

                                  rs1482596454 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>T [Show Flanks]
                                    Chromosome:
                                    6:65787987 (GRCh38)
                                    6:66497880 (GRCh37)
                                    Canonical SPDI:
                                    NC_000006.12:65787986:G:T
                                    Gene:
                                    SLC25A51P1 (Varview)
                                    Functional Consequence:
                                    non_coding_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000004/1 (TOPMED)
                                    T=0.000007/1 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1482534107 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      6:65788827 (GRCh38)
                                      6:66498720 (GRCh37)
                                      Canonical SPDI:
                                      NC_000006.12:65788826:G:A
                                      Gene:
                                      SLC25A51P1 (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      A=0./0 (ALFA)
                                      A=0.000007/1 (GnomAD)
                                      A=0.000011/3 (TOPMED)
                                      A=0.000342/1 (KOREAN)
                                      A=0.001451/24 (TOMMO)
                                      HGVS:

                                      19.

                                      rs1481978891 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>C [Show Flanks]
                                        Chromosome:
                                        6:65787041 (GRCh38)
                                        6:66496934 (GRCh37)
                                        Canonical SPDI:
                                        NC_000006.12:65787040:G:C
                                        Gene:
                                        SLC25A51P1 (Varview)
                                        Functional Consequence:
                                        2KB_upstream_variant,upstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000004/1 (TOPMED)
                                        C=0.000007/1 (GnomAD)
                                        C=0.000035/1 (TOMMO)
                                        HGVS:

                                        20.

                                        rs1480805080 [Homo sapiens]
                                          Variant type:
                                          DEL
                                          Alleles:
                                          GAG>- [Show Flanks]
                                          Chromosome:
                                          6:65786040 (GRCh38)
                                          6:66495933 (GRCh37)
                                          Canonical SPDI:
                                          NC_000006.12:65786039:GAG:
                                          Gene:
                                          SLC25A51P1 (Varview)
                                          Functional Consequence:
                                          2KB_upstream_variant,upstream_transcript_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          -=0.0011/5 (ALFA)
                                          -=0.0011/5 (Estonian)
                                          HGVS:

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