ClinVar Miner

List of variants in gene SH3TC2 reported as uncertain significance for not specified

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Total variants: 17
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NM_024577.3(SH3TC2):c.1138G>A (p.Gly380Arg) rs761184149
NM_024577.3(SH3TC2):c.1292T>A (p.Leu431His) rs1554121776
NM_024577.3(SH3TC2):c.1319G>A (p.Arg440His) rs755748579
NM_024577.3(SH3TC2):c.1326G>A (p.Pro442=) rs138967360
NM_024577.3(SH3TC2):c.1360A>G (p.Met454Val) rs1554121765
NM_024577.3(SH3TC2):c.1402_1403del (p.Ala468fs) rs876661068
NM_024577.3(SH3TC2):c.1402_1403delinsTT (p.Ala468Phe) rs863224780
NM_024577.3(SH3TC2):c.1483A>G (p.Thr495Ala) rs10077543
NM_024577.3(SH3TC2):c.148C>T (p.Pro50Ser) rs1057518369
NM_024577.3(SH3TC2):c.1537G>T (p.Ala513Ser) rs1554121737
NM_024577.3(SH3TC2):c.1651T>C (p.Phe551Leu) rs1554121720
NM_024577.3(SH3TC2):c.2812C>T (p.His938Tyr) rs144688852
NM_024577.3(SH3TC2):c.2954A>G (p.Glu985Gly) rs575937427
NM_024577.3(SH3TC2):c.2990G>A (p.Arg997Gln) rs140307699
NM_024577.3(SH3TC2):c.3313G>A (p.Val1105Met) rs750746661
NM_024577.3(SH3TC2):c.3686A>T (p.Asp1229Val) rs146920285
NM_024577.3(SH3TC2):c.73G>T (p.Asp25Tyr) rs10066882

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