ClinVar Miner

List of variants in gene TPM1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP gnomAD frequency
NM_001018005.2(TPM1):c.240+3941C>T rs4075584 0.82045
NM_001018005.2(TPM1):c.852-243T>G rs28583444 0.80998
NM_001018005.2(TPM1):c.375-75A>G rs4775614 0.80647
NM_001018005.2(TPM1):c.375-274G>A rs4238372 0.80592
NM_001018005.2(TPM1):c.564-152C>A rs4774472 0.79127
NM_001018005.2(TPM1):c.374+247C>T rs7173072 0.66537
NM_001018005.2(TPM1):c.453C>A (p.Ala151=) rs1071646 0.64628
NM_000366.2(TPM1):c.*287G= rs8519 0.64054
NM_001018005.2(TPM1):c.492+213G>A rs3803501 0.52628
NM_001018005.2(TPM1):c.241-88G>A rs4775613 0.52013
NM_001018005.2(TPM1):c.772+248C>G rs12442826 0.22492
NM_001018005.1(TPM1):c.-341G>C rs35829897 0.18390
NM_001018005.2(TPM1):c.240+4887G>C rs66793829 0.16803
NM_001018004.2(TPM1):c.773-276T>C rs9920576 0.13007
NM_000366.2(TPM1):c.*264C>T rs1050255 0.12938
NM_001018005.2(TPM1):c.241-52T>A rs28485524 0.12769
NM_001018005.1(TPM1):c.-331C>G rs8042834 0.12743
NM_001018005.1(TPM1):c.-394C>G rs3825973 0.12517
NM_001018005.2(TPM1):c.773-82G>A rs28660606 0.12406
NM_001018005.2(TPM1):c.851+196A>G rs28730803 0.11305
NM_001018005.1(TPM1):c.-420C>G rs3809568 0.11226
NM_001018005.1(TPM1):c.-509C>A rs3809567 0.11181
NM_001018005.2(TPM1):c.240+4722C>A rs11856618 0.07440
NM_001018005.2(TPM1):c.115-127C>G rs62013181 0.06261
NM_001018004.2(TPM1):c.773-910G>T rs2414814 0.05300
NM_001018005.2(TPM1):c.486T>C (p.Tyr162=) rs11558747 0.05001
NM_001018005.2(TPM1):c.*148G>T rs7668 0.03733
NM_001018005.2(TPM1):c.375-159C>T rs73440404 0.02340
NM_001018004.2(TPM1):c.773-266C>A rs11632190 0.02198
NM_001018004.2(TPM1):c.773-764G>A rs113519012 0.02078
NM_001018005.2(TPM1):c.851+41A>T rs3218718 0.00804
NM_001018020.2(TPM1):c.*31G>A rs11558748 0.00598
NM_001018005.2(TPM1):c.*76A>G rs140658011 0.00339
NM_001018005.2(TPM1):c.180C>T (p.Tyr60=) rs17850194 0.00273
NM_001018005.1(TPM1):c.-206G>A rs17525848 0.00111
NM_001018005.2(TPM1):c.115-262C>T rs74573041 0.00079
NM_001018005.2(TPM1):c.115-319C>G rs201720832 0.00070
NM_001018005.2(TPM1):c.*68A>G rs374459540 0.00054
NM_001018005.2(TPM1):c.*128C>T rs540306699 0.00049
NM_001018005.2(TPM1):c.851+44C>A rs191558659 0.00048
NM_001018005.2(TPM1):c.115-331C>T rs562829514 0.00041
NM_001018005.2(TPM1):c.177A>G (p.Lys59=) rs149346709 0.00031
NM_001018005.2(TPM1):c.375-5T>C rs377061868 0.00029
NM_001018005.2(TPM1):c.563+313A>G rs144700226 0.00029
NM_001018005.2(TPM1):c.115-214C>G rs947201175 0.00021
NM_001018005.2(TPM1):c.115-316G>A rs397516491 0.00015
NM_001018005.2(TPM1):c.114+14C>T rs576659891 0.00014
NM_001018005.2(TPM1):c.726G>A (p.Ala242=) rs200484871 0.00011
NM_001018005.2(TPM1):c.522C>T (p.Ser174=) rs200173919 0.00010
NM_001018005.2(TPM1):c.851+33C>T rs376843038 0.00009
NM_001018005.2(TPM1):c.564-11G>A rs532254032 0.00007
NM_001018005.2(TPM1):c.115-335G>T rs587780971 0.00006
NM_001018005.2(TPM1):c.27G>A (p.Gln9=) rs397516365 0.00006
NM_001018005.2(TPM1):c.493-18T>G rs377726678 0.00006
NM_001018005.2(TPM1):c.249C>T (p.Ala83=) rs200257214 0.00004
NM_001018005.2(TPM1):c.375-3C>T rs202228866 0.00003
NM_001018005.2(TPM1):c.663T>C (p.Tyr221=) rs774859181 0.00002
NC_000015.10:g.63042705C>G rs957045052 0.00001
NM_001018005.2(TPM1):c.-73C>T rs930569425 0.00001
NC_000015.10:g.63042641A>G rs2140590196
NC_000015.10:g.63042678T>G rs2140590601
NM_000366.2(TPM1):c.*30C>T rs114002706
NM_000366.2(TPM1):c.*30_*36insATTTT rs201620283
NM_000366.2(TPM1):c.*30_*36insATTTTGTTTT rs201620283
NM_001018004.2(TPM1):c.773-1110G>A rs73440433
NM_001018005.1(TPM1):c.-185G>C rs1032357917
NM_001018005.1(TPM1):c.-186G>A rs541046450
NM_001018005.2(TPM1):c.-14T>C rs2140593560
NM_001018005.2(TPM1):c.114+185_114+186insTGT rs34102093
NM_001018005.2(TPM1):c.115-339G>C rs756175447
NM_001018005.2(TPM1):c.148C>A (p.Leu50Ile) rs1060501866
NM_001018005.2(TPM1):c.241-317AAAAC[3] rs10603464
NM_001018005.2(TPM1):c.492+261G>T rs3803502
NM_001018005.2(TPM1):c.61C>A (p.Arg21=) rs1437698471
NM_001018005.2(TPM1):c.639+13del rs397516488
NM_001018005.2(TPM1):c.852-49del rs58304847
NM_001018005.2(TPM1):c.852-49dup rs58304847
NM_001018005.2(TPM1):c.87G>A (p.Lys29=) rs530234301

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