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1.

rs1491518085 has merged into rs34495040 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    GTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
    Chromosome:
    1:248680980 (GRCh38)
    1:248844281 (GRCh37)
    Canonical SPDI:
    NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000001.11:248680967:GTGTGTGTGTGTGTGTGTGTGTGTGTGT:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
    Gene:
    OR14I1 (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    GTGTGTGTGTGT=0./0 (ALFA)
    GTGTGTGT=0.2069/1036 (1000Genomes)
    HGVS:
    NC_000001.11:g.248680968GT[6], NC_000001.11:g.248680968GT[7], NC_000001.11:g.248680968GT[8], NC_000001.11:g.248680968GT[10], NC_000001.11:g.248680968GT[11], NC_000001.11:g.248680968GT[12], NC_000001.11:g.248680968GT[13], NC_000001.11:g.248680968GT[15], NC_000001.11:g.248680968GT[16], NC_000001.11:g.248680968GT[17], NC_000001.11:g.248680968GT[18], NC_000001.11:g.248680968GT[19], NC_000001.11:g.248680968GT[20], NC_000001.11:g.248680968GT[21], NC_000001.11:g.248680968GT[22], NC_000001.11:g.248680968GT[23], NC_000001.11:g.248680968GT[24], NC_000001.11:g.248680968GT[25], NC_000001.10:g.248844269GT[6], NC_000001.10:g.248844269GT[7], NC_000001.10:g.248844269GT[8], NC_000001.10:g.248844269GT[10], NC_000001.10:g.248844269GT[11], NC_000001.10:g.248844269GT[12], NC_000001.10:g.248844269GT[13], NC_000001.10:g.248844269GT[15], NC_000001.10:g.248844269GT[16], NC_000001.10:g.248844269GT[17], NC_000001.10:g.248844269GT[18], NC_000001.10:g.248844269GT[19], NC_000001.10:g.248844269GT[20], NC_000001.10:g.248844269GT[21], NC_000001.10:g.248844269GT[22], NC_000001.10:g.248844269GT[23], NC_000001.10:g.248844269GT[24], NC_000001.10:g.248844269GT[25], NW_025791755.1:g.322646GT[12], NW_025791755.1:g.322646GT[13], NW_025791755.1:g.322646GT[14], NW_025791755.1:g.322646GT[16], NW_025791755.1:g.322646GT[17], NW_025791755.1:g.322646GT[18], NW_025791755.1:g.322646GT[19], NW_025791755.1:g.322646GT[21], NW_025791755.1:g.322646GT[22], NW_025791755.1:g.322646GT[23], NW_025791755.1:g.322646GT[24], NW_025791755.1:g.322646GT[25], NW_025791755.1:g.322646GT[26], NW_025791755.1:g.322646GT[27], NW_025791755.1:g.322646GT[28], NW_025791755.1:g.322646GT[29], NW_025791755.1:g.322646GT[30], NW_025791755.1:g.322646GT[31], NM_001004734.3:c.*374AC[6], NM_001004734.3:c.*374AC[7], NM_001004734.3:c.*374AC[8], NM_001004734.3:c.*374AC[10], NM_001004734.3:c.*374AC[11], NM_001004734.3:c.*374AC[12], NM_001004734.3:c.*374AC[13], NM_001004734.3:c.*374AC[15], NM_001004734.3:c.*374AC[16], NM_001004734.3:c.*374AC[17], NM_001004734.3:c.*374AC[18], NM_001004734.3:c.*374AC[19], NM_001004734.3:c.*374AC[20], NM_001004734.3:c.*374AC[21], NM_001004734.3:c.*374AC[22], NM_001004734.3:c.*374AC[23], NM_001004734.3:c.*374AC[24], NM_001004734.3:c.*374AC[25], NM_001004734.2:c.*374AC[6], NM_001004734.2:c.*374AC[7], NM_001004734.2:c.*374AC[8], NM_001004734.2:c.*374AC[10], NM_001004734.2:c.*374AC[11], NM_001004734.2:c.*374AC[12], NM_001004734.2:c.*374AC[13], NM_001004734.2:c.*374AC[15], NM_001004734.2:c.*374AC[16], NM_001004734.2:c.*374AC[17], NM_001004734.2:c.*374AC[18], NM_001004734.2:c.*374AC[19], NM_001004734.2:c.*374AC[20], NM_001004734.2:c.*374AC[21], NM_001004734.2:c.*374AC[22], NM_001004734.2:c.*374AC[23], NM_001004734.2:c.*374AC[24], NM_001004734.2:c.*374AC[25], XM_047420643.1:c.*374AC[6], XM_047420643.1:c.*374AC[7], XM_047420643.1:c.*374AC[8], XM_047420643.1:c.*374AC[10], XM_047420643.1:c.*374AC[11], XM_047420643.1:c.*374AC[12], XM_047420643.1:c.*374AC[13], XM_047420643.1:c.*374AC[15], XM_047420643.1:c.*374AC[16], XM_047420643.1:c.*374AC[17], XM_047420643.1:c.*374AC[18], XM_047420643.1:c.*374AC[19], XM_047420643.1:c.*374AC[20], XM_047420643.1:c.*374AC[21], XM_047420643.1:c.*374AC[22], XM_047420643.1:c.*374AC[23], XM_047420643.1:c.*374AC[24], XM_047420643.1:c.*374AC[25]

    2.

    rs1491291462 has merged into rs1553277282 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      ->CGTG,CGTGTG,CGTGTGTG,CGTGTGTGTG,GTGTGTGTGTGTGTG [Show Flanks]
      Chromosome:
      1:248680967 (GRCh38)
      1:248844269 (GRCh37)
      Canonical SPDI:
      NC_000001.11:248680967:G:GCGTG,NC_000001.11:248680967:G:GCGTGTG,NC_000001.11:248680967:G:GCGTGTGTG,NC_000001.11:248680967:G:GCGTGTGTGTG,NC_000001.11:248680967:G:GGTGTGTGTGTGTGTG
      Gene:
      OR14I1 (Varview)
      Functional Consequence:
      3_prime_UTR_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      GCGTGTG=0./0 (ALFA)
      HGVS:
      NC_000001.11:g.248680968_248680969insCGTG, NC_000001.11:g.248680968_248680969insCGTGTG, NC_000001.11:g.248680968_248680969insCGTGTGTG, NC_000001.11:g.248680968_248680969insCGTGTGTGTG, NC_000001.11:g.248680968_248680969insGTGTGTGTGTGTGTG, NC_000001.10:g.248844269_248844270insCGTG, NC_000001.10:g.248844269_248844270insCGTGTG, NC_000001.10:g.248844269_248844270insCGTGTGTG, NC_000001.10:g.248844269_248844270insCGTGTGTGTG, NC_000001.10:g.248844269_248844270insGTGTGTGTGTGTGTG, NW_025791755.1:g.322658_322659insCGTG, NW_025791755.1:g.322654_322658GT[2]GCGTGTG[1], NW_025791755.1:g.322652_322658GT[3]GCGTGTGTG[1], NW_025791755.1:g.322650_322658GT[4]GCGTGTGTGTG[1], NW_025791755.1:g.322646_322658GTGTGTGTGTGTG[2]TG[1], NM_001004734.3:c.*401_*402insACGC, NM_001004734.3:c.*401CA[2]CGC[1], NM_001004734.3:c.*401CA[3]CGC[1], NM_001004734.3:c.*401CA[4]CGC[1], NM_001004734.3:c.*401CA[7]CC[1], NM_001004734.2:c.*401_*402insACGC, NM_001004734.2:c.*401CA[2]CGC[1], NM_001004734.2:c.*401CA[3]CGC[1], NM_001004734.2:c.*401CA[4]CGC[1], NM_001004734.2:c.*401CA[7]CC[1], XM_047420643.1:c.*401_*402insACGC, XM_047420643.1:c.*401CA[2]CGC[1], XM_047420643.1:c.*401CA[3]CGC[1], XM_047420643.1:c.*401CA[4]CGC[1], XM_047420643.1:c.*401CA[7]CC[1]

      3.

      rs1490751226 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>C,G [Show Flanks]
        Chromosome:
        1:248681100 (GRCh38)
        1:248844401 (GRCh37)
        Canonical SPDI:
        NC_000001.11:248681099:A:C,NC_000001.11:248681099:A:G
        Gene:
        OR14I1 (Varview)
        Functional Consequence:
        3_prime_UTR_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0./0 (ALFA)
        HGVS:

        4.

        rs1490574433 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>C [Show Flanks]
          Chromosome:
          1:248682777 (GRCh38)
          1:248846078 (GRCh37)
          Canonical SPDI:
          NC_000001.11:248682776:G:C
          Gene:
          OR14I1 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          C=0./0 (ALFA)
          C=0.000043/6 (GnomAD)
          HGVS:

          5.

          rs1490202397 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            1:248681481 (GRCh38)
            1:248844782 (GRCh37)
            Canonical SPDI:
            NC_000001.11:248681480:G:A
            Gene:
            OR14I1 (Varview)
            Functional Consequence:
            missense_variant,coding_sequence_variant
            Validated:
            by frequency
            MAF:
            A=0.000004/1 (GnomAD_exomes)
            HGVS:

            6.

            rs1489556916 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>G [Show Flanks]
              Chromosome:
              1:248685825 (GRCh38)
              1:248849126 (GRCh37)
              Canonical SPDI:
              NC_000001.11:248685824:T:G
              Gene:
              OR14I1 (Varview)
              Functional Consequence:
              intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              G=0./0 (ALFA)
              G=0.000004/1 (TOPMED)
              G=0.000007/1 (GnomAD)
              HGVS:

              7.

              rs1489442006 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>A,T [Show Flanks]
                Chromosome:
                1:248684787 (GRCh38)
                1:248848088 (GRCh37)
                Canonical SPDI:
                NC_000001.11:248684786:C:A,NC_000001.11:248684786:C:T
                Gene:
                OR14I1 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0./0 (ALFA)
                A=0.000015/2 (GnomAD)
                A=0.000026/7 (TOPMED)
                HGVS:

                8.

                rs1489276841 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>G [Show Flanks]
                  Chromosome:
                  1:248683382 (GRCh38)
                  1:248846683 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:248683381:C:G
                  Gene:
                  OR14I1 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000004/1 (TOPMED)
                  G=0.000007/1 (GnomAD)
                  HGVS:

                  9.

                  rs1487861450 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>C [Show Flanks]
                    Chromosome:
                    1:248687345 (GRCh38)
                    1:248850646 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:248687344:G:C
                    Gene:
                    OR14I1 (Varview)
                    Functional Consequence:
                    intron_variant,upstream_transcript_variant,genic_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)
                    HGVS:

                    10.

                    rs1487757249 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>T [Show Flanks]
                      Chromosome:
                      1:248682760 (GRCh38)
                      1:248846061 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:248682759:C:T
                      Gene:
                      OR14I1 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0./0 (ALFA)
                      T=0.000004/1 (TOPMED)
                      T=0.000007/1 (GnomAD)
                      HGVS:

                      11.

                      rs1487673974 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>C [Show Flanks]
                        Chromosome:
                        1:248682289 (GRCh38)
                        1:248845590 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:248682288:T:C
                        Gene:
                        OR14I1 (Varview)
                        Functional Consequence:
                        missense_variant,coding_sequence_variant
                        Validated:
                        by frequency
                        MAF:
                        C=0.000005/1 (GnomAD_exomes)
                        HGVS:

                        12.

                        rs1485923971 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>A [Show Flanks]
                          Chromosome:
                          1:248683652 (GRCh38)
                          1:248846953 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:248683651:T:A
                          Gene:
                          OR14I1 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000015/4 (TOPMED)
                          A=0.000021/3 (GnomAD)
                          A=0.000071/2 (TOMMO)
                          HGVS:

                          13.

                          rs1485050213 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>G [Show Flanks]
                            Chromosome:
                            1:248686767 (GRCh38)
                            1:248850068 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:248686766:T:G
                            Gene:
                            OR14I1 (Varview)
                            Functional Consequence:
                            intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            G=0.0005/2 (ALFA)
                            G=0.0005/2 (Estonian)
                            HGVS:

                            14.

                            rs1484979359 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A,T [Show Flanks]
                              Chromosome:
                              1:248685665 (GRCh38)
                              1:248848966 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:248685664:G:A,NC_000001.11:248685664:G:T
                              Gene:
                              OR14I1 (Varview)
                              Functional Consequence:
                              intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              T=0./0 (ALFA)
                              T=0.000007/1 (GnomAD)
                              HGVS:

                              15.

                              rs1484436360 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                1:248684760 (GRCh38)
                                1:248848061 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:248684759:A:G
                                Gene:
                                OR14I1 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                G=0./0 (ALFA)
                                HGVS:

                                16.

                                rs1484286069 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  1:248686455 (GRCh38)
                                  1:248849756 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:248686454:C:T
                                  Gene:
                                  OR14I1 (Varview)
                                  Functional Consequence:
                                  intron_variant,upstream_transcript_variant,genic_upstream_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:

                                  17.

                                  rs1484132833 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C [Show Flanks]
                                    Chromosome:
                                    1:248686090 (GRCh38)
                                    1:248849391 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:248686089:T:C
                                    Gene:
                                    OR14I1 (Varview)
                                    Functional Consequence:
                                    intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    C=0./0 (ALFA)
                                    C=0.000008/2 (TOPMED)
                                    HGVS:

                                    18.

                                    rs1483959323 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      1:248685613 (GRCh38)
                                      1:248848914 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:248685612:C:T
                                      Gene:
                                      OR14I1 (Varview)
                                      Functional Consequence:
                                      genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000007/1 (GnomAD)
                                      HGVS:

                                      19.

                                      rs1483308184 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>C [Show Flanks]
                                        Chromosome:
                                        1:248685956 (GRCh38)
                                        1:248849257 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:248685955:A:C
                                        Gene:
                                        OR14I1 (Varview)
                                        Functional Consequence:
                                        genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        C=0.000071/1 (ALFA)
                                        C=0.000004/1 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1481598640 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          1:248681844 (GRCh38)
                                          1:248845145 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:248681843:G:A
                                          Gene:
                                          OR14I1 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,missense_variant
                                          HGVS:

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