ClinVar Miner

List of variants in gene MYO7A studied for Hearing impairment

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_000260.4(MYO7A):c.2886G>C (p.Gln962His) rs200641606 0.00073
NM_000260.4(MYO7A):c.2798G>A (p.Arg933His) rs201489714 0.00029
NM_000260.4(MYO7A):c.4739A>G (p.Tyr1580Cys) rs370232066 0.00006
NM_000260.4(MYO7A):c.1399C>T (p.Arg467Trp) rs782073796 0.00003
NM_000260.4(MYO7A):c.3014C>T (p.Ala1005Val) rs113326082 0.00003
NM_000260.4(MYO7A):c.5900G>A (p.Arg1967Gln) rs752881271 0.00003
NM_000260.4(MYO7A):c.5291A>G (p.Glu1764Gly) rs759346941 0.00002
NM_000260.4(MYO7A):c.1144G>T (p.Val382Leu) rs782440130 0.00001
NM_000260.4(MYO7A):c.1792G>A (p.Ala598Thr) rs566111152 0.00001
NM_000260.4(MYO7A):c.5786A>G (p.Gln1929Arg) rs748331176 0.00001
NM_000260.4(MYO7A):c.1021C>G (p.Leu341Val) rs782765242
NM_000260.4(MYO7A):c.1211G>A (p.Gly404Glu) rs973746837
NM_000260.4(MYO7A):c.152A>C (p.Gln51Pro) rs375662903
NM_000260.4(MYO7A):c.2386C>T (p.Arg796Trp) rs111033339
NM_000260.4(MYO7A):c.2666C>T (p.Ala889Val) rs2135478407
NM_000260.4(MYO7A):c.3958A>G (p.Met1320Val) rs2135575353
NM_000260.4(MYO7A):c.3992A>G (p.Lys1331Arg) rs2135575658
NM_000260.4(MYO7A):c.4107G>T (p.Gln1369His) rs1565440220
NM_000260.4(MYO7A):c.4442-1G>C rs1485456037

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