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Links from Protein

Items: 2

1.

rs1461582363 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    1:247739151 (GRCh38)
    1:247902453 (GRCh37)
    Canonical SPDI:
    NC_000001.11:247739150:C:T
    Gene:
    OR14K1 (Varview), OR14A2 (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant,intron_variant
    Validated:
    by frequency,by cluster
    MAF:
    T=0.000004/1 (GnomAD_exomes)
    HGVS:
    2.

    rs1361790337 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      1:247739328 (GRCh38)
      1:247902630 (GRCh37)
      Canonical SPDI:
      NC_000001.11:247739327:C:T
      Gene:
      OR14K1 (Varview), OR14A2 (Varview)
      Functional Consequence:
      intron_variant,coding_sequence_variant,synonymous_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0./0 (ALFA)
      T=0.000007/1 (GnomAD)
      HGVS:

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