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Items: 3

1.

rs1266503 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,T [Show Flanks]
    Chromosome:
    19:19624448
    Gene:
    LPAR2 (Varview)
    Functional Consequence:
    coding_sequence_variant,synonymous_variant
    Validated:
    by frequency,by cluster
    MAF:
    G=0./0 (1000Genomes)
    G=0./0 (ALSPAC)
    G=0./0 (ExAC)
    G=0./0 (NorthernSweden)
    G=0./0 (TWINSUK)
    G=0./0 (Vietnamese)
    G=0.000008/2 (GnomAD_exomes)
    G=0.000016/2 (TOPMED)
    HGVS:
    NC_000019.10:g.19624448G>A, NC_000019.10:g.19624448G>T, NC_000019.9:g.19735257G>A, NC_000019.9:g.19735257G>T, NM_004720.6:c.864A>C, NM_004720.6:c.864A>T, NM_004720.5:c.864A>C, NM_004720.5:c.864A>T, XM_017027468.2:c.864C>T, XM_017027468.2:c.864C>A, XM_024451774.1:c.864C>T, XM_024451774.1:c.864C>A, XM_017027469.1:c.864C>T, XM_017027469.1:c.864C>A
    2.

    rs60787052 has merged into rs1266503 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A,T [Show Flanks]
      Chromosome:
      19:19624448
      Gene:
      LPAR2 (Varview)
      Functional Consequence:
      coding_sequence_variant,synonymous_variant
      Validated:
      by frequency,by cluster
      MAF:
      G=0./0 (1000Genomes)
      G=0./0 (ALSPAC)
      G=0./0 (ExAC)
      G=0./0 (NorthernSweden)
      G=0./0 (TWINSUK)
      G=0./0 (Vietnamese)
      G=0.000008/2 (GnomAD_exomes)
      G=0.000016/2 (TOPMED)
      HGVS:
      NC_000019.10:g.19624448G>A, NC_000019.10:g.19624448G>T, NC_000019.9:g.19735257G>A, NC_000019.9:g.19735257G>T, NM_004720.6:c.864A>C, NM_004720.6:c.864A>T, NM_004720.5:c.864A>C, NM_004720.5:c.864A>T, XM_017027468.2:c.864C>T, XM_017027468.2:c.864C>A, XM_024451774.1:c.864C>T, XM_024451774.1:c.864C>A, XM_017027469.1:c.864C>T, XM_017027469.1:c.864C>A
      3.

      rs17852282 has merged into rs1266503 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,T [Show Flanks]
        Chromosome:
        19:19624448
        Gene:
        LPAR2 (Varview)
        Functional Consequence:
        coding_sequence_variant,synonymous_variant
        Validated:
        by frequency,by cluster
        MAF:
        G=0./0 (1000Genomes)
        G=0./0 (ALSPAC)
        G=0./0 (ExAC)
        G=0./0 (NorthernSweden)
        G=0./0 (TWINSUK)
        G=0./0 (Vietnamese)
        G=0.000008/2 (GnomAD_exomes)
        G=0.000016/2 (TOPMED)
        HGVS:
        NC_000019.10:g.19624448G>A, NC_000019.10:g.19624448G>T, NC_000019.9:g.19735257G>A, NC_000019.9:g.19735257G>T, NM_004720.6:c.864A>C, NM_004720.6:c.864A>T, NM_004720.5:c.864A>C, NM_004720.5:c.864A>T, XM_017027468.2:c.864C>T, XM_017027468.2:c.864C>A, XM_024451774.1:c.864C>T, XM_024451774.1:c.864C>A, XM_017027469.1:c.864C>T, XM_017027469.1:c.864C>A

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