ClinVar Miner

List of variants in gene TPM1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_001018005.2(TPM1):c.851+233G>A rs73440420 0.02546
NM_001018004.2(TPM1):c.*119T>C rs138843544 0.02527
NM_001018005.2(TPM1):c.374+138A>C rs16946383 0.01495
NM_001018004.2(TPM1):c.773-1063T>C rs114073739 0.01299
NM_001018005.2(TPM1):c.492+218G>A rs75095143 0.01298
NM_001018005.1(TPM1):c.-272A>C rs879364664 0.01181
NM_001018005.1(TPM1):c.-264G>A rs528589173 0.01178
NM_001018005.2(TPM1):c.375-262G>A rs116860970 0.01050
NM_001018005.2(TPM1):c.241-167A>T rs114027732 0.01042
NC_000015.10:g.63042591C>T rs565301907 0.00959
NM_001018005.2(TPM1):c.493-110T>C rs4514624 0.00870
NM_001018005.2(TPM1):c.564-47C>T rs77362326 0.00782
NM_001018005.2(TPM1):c.639+22G>C rs28730802 0.00782
NM_001018004.2(TPM1):c.772+3543G>C rs74021742 0.00739
NM_001018005.2(TPM1):c.375-311C>T rs78809927 0.00732
NM_001018005.2(TPM1):c.240+3965del rs201173447 0.00701
NM_001018005.2(TPM1):c.851+189C>G rs111924332 0.00454
NM_001018005.2(TPM1):c.772+94_772+96del rs57598555 0.00285
NM_001018005.2(TPM1):c.772+163G>C rs190305952 0.00252
NM_001018005.2(TPM1):c.773-233G>A rs150284424 0.00223
NM_001018005.2(TPM1):c.240+4775G>T rs183030912 0.00119
NM_001018004.2(TPM1):c.775A>G (p.Lys259Glu) rs144045691 0.00052
NM_001018005.2(TPM1):c.851+6C>T rs375043184 0.00029
NM_001018004.2(TPM1):c.773-1117T>G rs141403692 0.00028
NM_001018005.2(TPM1):c.852-32T>G rs143877453 0.00025
NM_001018020.2(TPM1):c.835C>T (p.Leu279=) rs374434837 0.00013
NM_001018005.2(TPM1):c.773-3T>C rs113759732 0.00010
NM_001018005.2(TPM1):c.563+12C>T rs756230680 0.00009
NM_001018005.2(TPM1):c.563+7G>A rs374563216 0.00006
NM_001018005.2(TPM1):c.783C>T (p.Tyr261=) rs751001221 0.00004
NM_001018005.2(TPM1):c.549T>C (p.Ala183=) rs199476313 0.00003
NM_001018005.2(TPM1):c.563+347C>T rs759081217 0.00003
NM_001018005.2(TPM1):c.564-12C>T rs113591254 0.00003
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser) rs397516395 0.00003
NM_001018005.2(TPM1):c.240+11G>A rs367999295 0.00002
NM_001018005.2(TPM1):c.31C>T (p.Leu11=) rs766883758 0.00002
NM_001018005.2(TPM1):c.-41C>T rs1335948932 0.00001
NM_001018005.2(TPM1):c.115-189G>C rs1057520978 0.00001
NM_001018005.2(TPM1):c.115-244G>A rs989115520 0.00001
NM_001018005.2(TPM1):c.444G>C (p.Leu148=) rs376518788 0.00001
NM_001018005.2(TPM1):c.639+10G>A rs763272536 0.00001
NM_001018005.2(TPM1):c.705T>C (p.Ala235=) rs1222579354 0.00001
NM_001018005.2(TPM1):c.773-18T>C rs759150466 0.00001
NM_001018005.2(TPM1):c.837C>T (p.Asn279=) rs397516393 0.00001
NM_001018005.2(TPM1):c.840T>C (p.Asp280=) rs749271066 0.00001
NC_000015.10:g.63042556_63042557insAGGGCCG rs879682441
NM_000366.2(TPM1):c.849C>T (p.Asn283=) rs1057521824
NM_001018004.2(TPM1):c.772+3552T>C rs150926100
NM_001018005.2(TPM1):c.115-238G>C rs730881126
NM_001018005.2(TPM1):c.144G>A (p.Lys48=) rs1555403374
NM_001018005.2(TPM1):c.375-17C>T rs1057523797
NM_001018005.2(TPM1):c.493-234T>G rs79297374
NM_001018005.2(TPM1):c.563+243C>T rs1596379300
NM_001018005.2(TPM1):c.772+99del rs58882433
NM_001018005.2(TPM1):c.775G>C (p.Glu259Gln) rs397516389
NM_001018005.2(TPM1):c.851+6C>A rs375043184

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