ClinVar Miner

List of variants in gene POMT1 reported as uncertain significance by Athena Diagnostics Inc

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_001077365.2(POMT1):c.1064T>C (p.Ile355Thr) rs1334264954
NM_001077365.2(POMT1):c.1117G>C (p.Val373Leu) rs200508760
NM_001077365.2(POMT1):c.1150G>A (p.Gly384Ser) rs146234177
NM_001077365.2(POMT1):c.1190C>A (p.Ala397Asp) rs1564364465
NM_001077365.2(POMT1):c.1354G>A (p.Ala452Thr) rs150702948
NM_001077365.2(POMT1):c.1451C>T (p.Thr484Met) rs201220016
NM_001077365.2(POMT1):c.1484C>T (p.Ala495Val) rs761439623
NM_001077365.2(POMT1):c.1598C>T (p.Ala533Val) rs199682341
NM_001077365.2(POMT1):c.1601T>C (p.Leu534Pro) rs1489617043
NM_001077365.2(POMT1):c.1729A>G (p.Ile577Val) rs749978093
NM_001077365.2(POMT1):c.178T>C (p.Phe60Leu) rs1564332130
NM_001077365.2(POMT1):c.1793G>A (p.Arg598Gln) rs202140413
NM_001077365.2(POMT1):c.1828G>A (p.Ala610Thr) rs773190071
NM_001077365.2(POMT1):c.2068G>A (p.Val690Met) rs150209587
NM_001077365.2(POMT1):c.2132C>T (p.Ala711Val) rs769694503
NM_001077365.2(POMT1):c.426C>T (p.Ile142=) rs771390000
NM_001077365.2(POMT1):c.539+3A>C rs780457748
NM_001077365.2(POMT1):c.586G>A (p.Ala196Thr) rs199498900
NM_001077365.2(POMT1):c.699+14T>A rs370038491
NM_001077365.2(POMT1):c.781G>A (p.Val261Ile) rs759734493
NM_001077365.2(POMT1):c.847A>C (p.Ser283Arg) rs747506380

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