ClinVar Miner

List of variants in gene TPM1 reported as uncertain significance for not specified

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Total variants: 60
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HGVS dbSNP
NM_001018004.2(TPM1):c.773-1187G>A rs144451403
NM_001018004.2(TPM1):c.775A>G (p.Lys259Glu) rs144045691
NM_001018005.2(TPM1):c.*5_*8del rs786204415
NM_001018005.2(TPM1):c.115-238G>C rs730881126
NM_001018005.2(TPM1):c.118G>T (p.Glu40Ter) rs104894501
NM_001018005.2(TPM1):c.14_16AGA[2] (p.Lys7del) rs730881155
NM_001018005.2(TPM1):c.14_16AGA[4] (p.Lys7dup) rs730881155
NM_001018005.2(TPM1):c.240+1G>A rs730881146
NM_001018005.2(TPM1):c.240+3A>C rs1555403436
NM_001018005.2(TPM1):c.252C>G (p.Asp84Glu) rs369617788
NM_001018005.2(TPM1):c.2del (p.Met1fs) rs397516366
NM_001018005.2(TPM1):c.305C>A (p.Ala102Asp) rs397516367
NM_001018005.2(TPM1):c.343G>A (p.Glu115Lys) rs727504313
NM_001018005.2(TPM1):c.364G>A (p.Glu122Lys) rs876658031
NM_001018005.2(TPM1):c.389T>C (p.Ile130Thr) rs727503517
NM_001018005.2(TPM1):c.424G>A (p.Glu142Lys) rs1555408649
NM_001018005.2(TPM1):c.458A>G (p.His153Arg) rs727505043
NM_001018005.2(TPM1):c.45G>T (p.Lys15Asn) rs199476301
NM_001018005.2(TPM1):c.460A>G (p.Ile154Val) rs1555408679
NM_001018005.2(TPM1):c.475G>A (p.Asp159Asn) rs397516373
NM_001018005.2(TPM1):c.493-6C>T rs397516374
NM_001018005.2(TPM1):c.508G>A (p.Val170Ile) rs1555409095
NM_001018005.2(TPM1):c.533G>A (p.Arg178His) rs397516375
NM_001018005.2(TPM1):c.548C>T (p.Ala183Val) rs397516376
NM_001018005.2(TPM1):c.563+249C>T rs397516379
NM_001018005.2(TPM1):c.563+254A>G rs397516380
NM_001018005.2(TPM1):c.563+308A>C rs1555409301
NM_001018005.2(TPM1):c.563_563+1insCCAA rs1060499914
NM_001018005.2(TPM1):c.564-11G>A rs532254032
NM_001018005.2(TPM1):c.58G>A (p.Asp20Asn) rs727504391
NM_001018005.2(TPM1):c.632C>G (p.Ala211Gly) rs397516487
NM_001018005.2(TPM1):c.644C>T (p.Ser215Leu) rs199476316
NM_001018005.2(TPM1):c.64G>A (p.Ala22Thr) rs397516382
NM_001018005.2(TPM1):c.673A>G (p.Ile225Val) rs193922410
NM_001018005.2(TPM1):c.676A>C (p.Lys226Gln) rs397516383
NM_001018005.2(TPM1):c.692A>G (p.Lys231Arg) rs397516385
NM_001018005.2(TPM1):c.69G>C (p.Glu23Asp) rs876661396
NM_001018005.2(TPM1):c.712C>T (p.Arg238Trp) rs397516386
NM_001018005.2(TPM1):c.725C>T (p.Ala242Val) rs397516387
NM_001018005.2(TPM1):c.734C>T (p.Ser245Leu) rs397516388
NM_001018005.2(TPM1):c.762T>A (p.Asp254Glu) rs727504354
NM_001018005.2(TPM1):c.762T>G (p.Asp254Glu) rs727504354
NM_001018005.2(TPM1):c.775G>A (p.Glu259Lys) rs397516389
NM_001018005.2(TPM1):c.790A>G (p.Lys264Glu) rs397516390
NM_001018005.2(TPM1):c.797A>G (p.Lys266Arg) rs371934474
NM_001018005.2(TPM1):c.802A>G (p.Lys268Glu) rs1555410433
NM_001018005.2(TPM1):c.815A>C (p.Glu272Ala) rs727503519
NM_001018005.2(TPM1):c.829G>A (p.Ala277Thr) rs149659674
NM_001018005.2(TPM1):c.82G>A (p.Asp28Asn) rs397516391
NM_001018005.2(TPM1):c.82G>C (p.Asp28His) rs397516391
NM_001018005.2(TPM1):c.830C>G (p.Ala277Gly) rs199476320
NM_001018005.2(TPM1):c.835A>C (p.Asn279His) rs397516392
NM_001018005.2(TPM1):c.841A>G (p.Met281Val) rs397516394
NM_001018005.2(TPM1):c.842T>C (p.Met281Thr) rs199476321
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser) rs397516395
NM_001018005.2(TPM1):c.850A>G (p.Ile284Val) rs199476322
NM_001018005.2(TPM1):c.851+15A>G rs876658030
NM_001018005.2(TPM1):c.91G>A (p.Ala31Thr) rs397516396
NM_001018005.2(TPM1):c.97G>A (p.Glu33Lys) rs397516397
NM_001018008.2(TPM1):c.695G>A (p.Arg232His) rs730881128

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