ClinVar Miner

List of variants in gene TPM1 studied for not provided

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Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP
NM_000366.5(TPM1):c.202C>A (p.Gln68Lys)
NM_000366.5(TPM1):c.835A>C (p.Asn279His) rs397516392
NM_001018005.1(TPM1):c.104G>C (p.Arg35Thr) rs730881152
NM_001018005.1(TPM1):c.109A>G (p.Lys37Glu) rs199476303
NM_001018005.1(TPM1):c.10A>G (p.Ile4Val) rs730881148
NM_001018005.1(TPM1):c.115-204G>C rs730881133
NM_001018005.1(TPM1):c.115-206C>A rs1555403294
NM_001018005.1(TPM1):c.115-275A>T rs730881132
NM_001018005.1(TPM1):c.118G>C (p.Glu40Gln) rs104894501
NM_001018005.1(TPM1):c.118G>T (p.Glu40Ter) rs104894501
NM_001018005.1(TPM1):c.154G>A (p.Gly52Ser) rs730881127
NM_001018005.1(TPM1):c.160G>A (p.Glu54Lys) rs104894505
NM_001018005.1(TPM1):c.172G>C (p.Asp58His) rs199476304
NM_001018005.1(TPM1):c.184G>C (p.Glu62Gln) rs199476305
NM_001018005.1(TPM1):c.187G>A (p.Ala63Thr) rs1064796782
NM_001018005.1(TPM1):c.188C>T (p.Ala63Val) rs199476306
NM_001018005.1(TPM1):c.209A>C (p.Lys70Thr) rs199476307
NM_001018005.1(TPM1):c.211C>G (p.Leu71Val) rs730881143
NM_001018005.1(TPM1):c.240+1G>A rs730881146
NM_001018005.1(TPM1):c.241-12_241-11delCTinsTG rs199476309
NM_001018005.1(TPM1):c.248C>A (p.Ala83Asp) rs730881130
NM_001018005.1(TPM1):c.253G>T (p.Val85Leu) rs730881156
NM_001018005.1(TPM1):c.25C>A (p.Gln9Lys) rs730881149
NM_001018005.1(TPM1):c.267C>G (p.Asn89Lys) rs1085307487
NM_001018005.1(TPM1):c.26A>T (p.Gln9Leu) rs1555402931
NM_001018005.1(TPM1):c.275T>C (p.Ile92Thr) rs199476310
NM_001018005.1(TPM1):c.276C>G (p.Ile92Met) rs730881157
NM_001018005.1(TPM1):c.284T>C (p.Val95Ala) rs104894504
NM_001018005.1(TPM1):c.289G>C (p.Glu97Gln) rs1064793284
NM_001018005.1(TPM1):c.337C>G (p.Leu113Val) rs397516369
NM_001018005.1(TPM1):c.343G>A (p.Glu115Lys) rs727504313
NM_001018005.1(TPM1):c.381G>A (p.Met127Ile) rs201211957
NM_001018005.1(TPM1):c.389T>C (p.Ile130Thr) rs727503517
NM_001018005.1(TPM1):c.403C>A (p.Gln135Lys) rs11558749
NM_001018005.1(TPM1):c.407_409delAAG (p.Lys136_Asp137delinsAsn) rs1064797199
NM_001018005.1(TPM1):c.40G>T (p.Asp14Tyr) rs876661210
NM_001018005.1(TPM1):c.410A>T (p.Asp137Val) rs730881134
NM_001018005.1(TPM1):c.411T>A (p.Asp137Glu) rs1555408631
NM_001018005.1(TPM1):c.418A>C (p.Lys140Gln) rs730881135
NM_001018005.1(TPM1):c.428T>A (p.Ile143Asn)
NM_001018005.1(TPM1):c.428T>G (p.Ile143Ser) rs730881136
NM_001018005.1(TPM1):c.453C>A (p.Ala151=) rs1071646
NM_001018005.1(TPM1):c.45G>T (p.Lys15Asn) rs199476301
NM_001018005.1(TPM1):c.46G>C (p.Glu16Gln) rs727504290
NM_001018005.1(TPM1):c.475G>A (p.Asp159Asn) rs397516373
NM_001018005.1(TPM1):c.479G>A (p.Arg160His) rs199476311
NM_001018005.1(TPM1):c.486T>C (p.Tyr162=) rs11558747
NM_001018005.1(TPM1):c.513C>G (p.Ile171Met) rs730881137
NM_001018005.1(TPM1):c.514A>C (p.Ile172Leu) rs760374266
NM_001018005.1(TPM1):c.515T>C (p.Ile172Thr) rs199476312
NM_001018005.1(TPM1):c.516T>G (p.Ile172Met) rs730881138
NM_001018005.1(TPM1):c.523G>A (p.Asp175Asn) rs104894503
NM_001018005.1(TPM1):c.539A>G (p.Glu180Gly) rs104894502
NM_001018005.1(TPM1):c.539A>T (p.Glu180Val) rs104894502
NM_001018005.1(TPM1):c.548C>T (p.Ala183Val) rs397516376
NM_001018005.1(TPM1):c.549T>G (p.Ala183=) rs199476313
NM_001018005.1(TPM1):c.551delA (p.Glu184Glyfs) rs730881153
NM_001018005.1(TPM1):c.554T>G (p.Leu185Arg) rs199476314
NM_001018005.1(TPM1):c.563+10_563+13delinsACCA
NM_001018005.1(TPM1):c.563+266C>T rs201813515
NM_001018005.1(TPM1):c.572_573delCCinsTT (p.Ala191Val) rs730881154
NM_001018005.1(TPM1):c.574G>A (p.Glu192Lys) rs199476315
NM_001018005.1(TPM1):c.58G>A (p.Asp20Asn) rs727504391
NM_001018005.1(TPM1):c.592A>G (p.Lys198Glu) rs730881140
NM_001018005.1(TPM1):c.602C>T (p.Thr201Met) rs730881141
NM_001018005.1(TPM1):c.61C= (p.Arg21=) rs1437698471
NM_001018005.1(TPM1):c.625G>A (p.Ala209Thr) rs730881159
NM_001018005.1(TPM1):c.62G>T (p.Arg21Leu) rs730881151
NM_001018005.1(TPM1):c.637A>C (p.Lys213Gln)
NM_001018005.1(TPM1):c.639+81A>T rs587777906
NM_001018005.1(TPM1):c.644C>T (p.Ser215Leu) rs199476316
NM_001018005.1(TPM1):c.64G>A (p.Ala22Thr) rs397516382
NM_001018005.1(TPM1):c.673A>G (p.Ile225Val) rs193922410
NM_001018005.1(TPM1):c.677A>G (p.Lys226Arg) rs730881144
NM_001018005.1(TPM1):c.67G>C (p.Glu23Gln) rs199476302
NM_001018005.1(TPM1):c.688G>A (p.Asp230Asn) rs199476317
NM_001018005.1(TPM1):c.702+4A>G rs730881145
NM_001018005.1(TPM1):c.715G>A (p.Ala239Thr) rs199476318
NM_001018005.1(TPM1):c.742A>G (p.Lys248Glu) rs199476319
NM_001018005.1(TPM1):c.743A>C (p.Lys248Thr) rs730881160
NM_001018005.1(TPM1):c.762T>G (p.Asp254Glu) rs727504354
NM_001018005.1(TPM1):c.787C>G (p.Gln263Glu) rs730881147
NM_001018005.1(TPM1):c.815A>G (p.Glu272Gly) rs727503519
NM_001018005.1(TPM1):c.82G>A (p.Asp28Asn) rs397516391
NM_001018005.1(TPM1):c.82G>C (p.Asp28His) rs397516391
NM_001018005.1(TPM1):c.830C>G (p.Ala277Gly) rs199476320
NM_001018005.1(TPM1):c.830C>T (p.Ala277Val) rs199476320
NM_001018005.1(TPM1):c.841A>G (p.Met281Val) rs397516394
NM_001018005.1(TPM1):c.842T>C (p.Met281Thr) rs199476321
NM_001018005.1(TPM1):c.850A>G (p.Ile284Val) rs199476322
NM_001018005.1(TPM1):c.98A>C (p.Glu33Ala) rs886039444
NM_001018006.1(TPM1):c.17A>G (p.Lys6Arg)

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