ClinVar Miner

List of variants in gene SLC37A4 reported as not provided

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Total variants: 32
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HGVS dbSNP
NM_001164277.1(SLC37A4):c.1015G>T (p.Gly339Cys) rs80356490
NM_001164277.1(SLC37A4):c.1016G>A (p.Gly339Asp) rs121908980
NM_001164277.1(SLC37A4):c.1099G>A (p.Ala367Thr) rs80356492
NM_001164277.1(SLC37A4):c.1118C>A (p.Ala373Asp) rs193302901
NM_001164277.1(SLC37A4):c.1126G>A (p.Gly376Ser) rs193302897
NM_001164277.1(SLC37A4):c.148G>C (p.Gly50Arg) rs193302894
NM_001164277.1(SLC37A4):c.149G>A (p.Gly50Glu) rs193302877
NM_001164277.1(SLC37A4):c.162C>A (p.Ser54Arg) rs193302898
NM_001164277.1(SLC37A4):c.163A>C (p.Ser55Arg) rs193302884
NM_001164277.1(SLC37A4):c.202G>A (p.Gly68Arg) rs193302885
NM_001164277.1(SLC37A4):c.254T>C (p.Leu85Pro) rs193302899
NM_001164277.1(SLC37A4):c.263G>A (p.Gly88Asp) rs193302886
NM_001164277.1(SLC37A4):c.352T>C (p.Trp118Arg) rs80356489
NM_001164277.1(SLC37A4):c.398A>C (p.Gln133Pro) rs193302896
NM_001164277.1(SLC37A4):c.443C>T (p.Ala148Val) rs193302879
NM_001164277.1(SLC37A4):c.446G>A (p.Gly149Glu) rs193302892
NM_001164277.1(SLC37A4):c.448G>A (p.Gly150Arg) rs193302883
NM_001164277.1(SLC37A4):c.458C>T (p.Pro153Leu) rs193302890
NM_001164277.1(SLC37A4):c.526T>C (p.Cys176Arg) rs193302895
NM_001164277.1(SLC37A4):c.547T>C (p.Cys183Arg) rs193302893
NM_001164277.1(SLC37A4):c.572C>T (p.Pro191Leu) rs193302888
NM_001164277.1(SLC37A4):c.59G>A (p.Gly20Asp) rs193302881
NM_001164277.1(SLC37A4):c.686T>C (p.Leu229Pro) rs193302902
NM_001164277.1(SLC37A4):c.70T>C (p.Tyr24His) rs193302887
NM_001164277.1(SLC37A4):c.736T>C (p.Trp246Arg) rs193302878
NM_001164277.1(SLC37A4):c.81T>A (p.Asn27Lys) rs193302889
NM_001164277.1(SLC37A4):c.82C>T (p.Arg28Cys) rs193302882
NM_001164277.1(SLC37A4):c.833T>A (p.Ile278Asn) rs193302900
NM_001164277.1(SLC37A4):c.83G>A (p.Arg28His) rs121908978
NM_001164277.1(SLC37A4):c.898C>T (p.Arg300Cys) rs193302880
NM_001164277.1(SLC37A4):c.899G>A (p.Arg300His) rs193302903
NM_001164277.1(SLC37A4):c.902A>C (p.His301Pro) rs193302891

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