ClinVar Miner

List of variants in gene CDKN2A reported as uncertain significance by Mendelics

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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_000077.5(CDKN2A):c.298G>T (p.Ala100Ser) rs200863613 0.00038
NM_058195.4(CDKN2A):c.160C>A (p.Arg54Ser) rs896054565 0.00006
NM_000077.5(CDKN2A):c.160A>C (p.Met54Leu) rs201314211 0.00005
NM_000077.5(CDKN2A):c.197A>G (p.His66Arg) rs756750256 0.00004
NM_000077.5(CDKN2A):c.315C>A (p.Asp105Glu) rs763269347 0.00001
NM_000077.5(CDKN2A):c.32C>T (p.Pro11Leu) rs1374664673 0.00001
NM_000077.5(CDKN2A):c.333C>T (p.Gly111=) rs1490202463 0.00001
NM_058195.4(CDKN2A):c.35G>A (p.Arg12Gln) rs201877069 0.00001
NM_000077.5(CDKN2A):c.148C>A (p.Gln50Lys) rs864622636
NM_000077.5(CDKN2A):c.150+82A>G rs1231900408
NM_000077.5(CDKN2A):c.170C>A (p.Ala57Asp) rs372266620
NM_000077.5(CDKN2A):c.220G>C (p.Asp74His) rs760640852
NM_000077.5(CDKN2A):c.221A>C (p.Asp74Ala) rs200429615
NM_000077.5(CDKN2A):c.26T>C (p.Met9Thr) rs145445140
NM_000077.5(CDKN2A):c.294C>T (p.His98=) rs752685118
NM_000077.5(CDKN2A):c.404G>C (p.Gly135Ala) rs1182554152

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