ClinVar Miner

List of variants in gene TPM1 reported as likely benign for not provided

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Total variants: 34
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HGVS dbSNP
NC_000015.10:g.63042558A>C
NC_000015.10:g.63042566G>A
NM_001018005.2(TPM1):c.177A>G (p.Lys59=) rs149346709
NM_001018005.2(TPM1):c.241-167A>T
NM_001018005.2(TPM1):c.241-9T>C rs377417143
NM_001018005.2(TPM1):c.374+138A>C
NM_001018005.2(TPM1):c.375-262G>A
NM_001018005.2(TPM1):c.375-311C>T
NM_001018005.2(TPM1):c.375-5T>C rs377061868
NM_001018005.2(TPM1):c.39C>G (p.Leu13=)
NM_001018005.2(TPM1):c.408A>G (p.Lys136=)
NM_001018005.2(TPM1):c.444G>C (p.Leu148=) rs376518788
NM_001018005.2(TPM1):c.474C>T (p.Ala158=)
NM_001018005.2(TPM1):c.493-110T>C
NM_001018005.2(TPM1):c.522C>T (p.Ser174=) rs200173919
NM_001018005.2(TPM1):c.563+243C>T
NM_001018005.2(TPM1):c.563+7G>A rs374563216
NM_001018005.2(TPM1):c.564-47C>T
NM_001018005.2(TPM1):c.564-5A>G
NM_001018005.2(TPM1):c.573C>T (p.Ala191=) rs780507307
NM_001018005.2(TPM1):c.639+22G>C
NM_001018005.2(TPM1):c.639+8A>G
NM_001018005.2(TPM1):c.684T>C (p.Leu228=) rs397516384
NM_001018005.2(TPM1):c.702+7T>A
NM_001018005.2(TPM1):c.702+7del rs1060504368
NM_001018005.2(TPM1):c.726G>A (p.Ala242=) rs200484871
NM_001018005.2(TPM1):c.773-233G>A
NM_001018005.2(TPM1):c.828C>T (p.His276=) rs368813394
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser) rs397516395
NM_001018005.2(TPM1):c.851+189C>G
NM_001018005.2(TPM1):c.851+233G>A
NM_001018005.2(TPM1):c.851+6C>T rs375043184
NM_001018005.2(TPM1):c.851+7G>A
NM_001018005.2(TPM1):c.87G>A (p.Lys29=)

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