ClinVar Miner

List of variants in gene TMPRSS3 reported as uncertain significance for not specified

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_001256317.3(TMPRSS3):c.1360T>C (p.Ter454Arg) rs149919890 0.00098
NM_001256317.3(TMPRSS3):c.412G>A (p.Ala138Thr) rs140614903 0.00054
NM_001256317.3(TMPRSS3):c.47G>A (p.Arg16Gln) rs369418733 0.00013
NM_001256317.3(TMPRSS3):c.280G>A (p.Gly94Arg) rs143762350 0.00011
NM_001256317.3(TMPRSS3):c.616+5G>A rs138768408 0.00009
NM_001256317.3(TMPRSS3):c.1169C>T (p.Thr390Met) rs145766262 0.00006
NM_001256317.3(TMPRSS3):c.1120G>A (p.Val374Met) rs775508015 0.00002
NM_001256317.3(TMPRSS3):c.763G>T (p.Ala255Ser) rs778263709 0.00002
NM_001256317.3(TMPRSS3):c.1000G>A (p.Asp334Asn) rs776873836 0.00001
NM_001256317.3(TMPRSS3):c.1054G>A (p.Ala352Thr) rs188750127 0.00001
NM_001256317.3(TMPRSS3):c.1197C>G (p.Asp399Glu) rs397517371 0.00001
NM_001256317.3(TMPRSS3):c.1344+3G>A rs751001285 0.00001
NM_001256317.3(TMPRSS3):c.298G>C (p.Asp100His) rs397517374 0.00001
NM_001256317.3(TMPRSS3):c.446+4A>T rs376253981 0.00001
NM_001256317.3(TMPRSS3):c.677C>T (p.Ser226Leu) rs763150678 0.00001
NM_001256317.3(TMPRSS3):c.731G>T (p.Gly244Val) rs397517377 0.00001
NM_001256317.3(TMPRSS3):c.783-13C>A rs140443203 0.00001
NM_001256317.3(TMPRSS3):c.1087T>G (p.Leu363Val) rs397517370
NM_001256317.3(TMPRSS3):c.1149G>T (p.Met383Ile) rs727503492
NM_001256317.3(TMPRSS3):c.1180G>C (p.Asp394His) rs111033537
NM_001256317.3(TMPRSS3):c.1250C>T (p.Ala417Val)
NM_001256317.3(TMPRSS3):c.1283A>G (p.Asn428Ser)
NM_001256317.3(TMPRSS3):c.1303C>G (p.Arg435Gly) rs565348874
NM_001256317.3(TMPRSS3):c.234A>C (p.Arg78Ser) rs567503320
NM_001256317.3(TMPRSS3):c.238C>T (p.Arg80Cys) rs143733205
NM_001256317.3(TMPRSS3):c.257T>A (p.Ile86Asn) rs397517372
NM_001256317.3(TMPRSS3):c.272G>A (p.Arg91Gln) rs397517373
NM_001256317.3(TMPRSS3):c.550T>G (p.Leu184Val) rs876658022
NM_001256317.3(TMPRSS3):c.613A>C (p.Thr205Pro) rs1175336303
NM_001256317.3(TMPRSS3):c.948C>G (p.Phe316Leu) rs727504592

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