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: 23
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HGVS dbSNP
NC_000015.10:g.63042321C>A
NC_000015.10:g.63042410C>G
NC_000015.10:g.63042436C>G
NC_000015.10:g.63042489G>C
NC_000015.10:g.63042499C>G
NM_001018005.2(TPM1):c.114+14C>T rs576659891
NM_001018005.2(TPM1):c.115-335G>T rs587780971
NM_001018005.2(TPM1):c.180C>T (p.Tyr60=) rs17850194
NM_001018005.2(TPM1):c.374+247C>T
NM_001018005.2(TPM1):c.375-274G>A
NM_001018005.2(TPM1):c.375-3C>T rs202228866
NM_001018005.2(TPM1):c.453C>A (p.Ala151=) rs1071646
NM_001018005.2(TPM1):c.486T>C (p.Tyr162=) rs11558747
NM_001018005.2(TPM1):c.492+213G>A
NM_001018005.2(TPM1):c.492+261G>T
NM_001018005.2(TPM1):c.563+313A>G rs144700226
NM_001018005.2(TPM1):c.564-11G>A rs532254032
NM_001018005.2(TPM1):c.61C>A (p.Arg21=) rs1437698471
NM_001018005.2(TPM1):c.639+13del rs397516488
NM_001018005.2(TPM1):c.772+248C>G
NM_001018005.2(TPM1):c.851+196A>G
NM_001018005.2(TPM1):c.851+33C>T rs376843038
NM_001018005.2(TPM1):c.852-243T>G

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