ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP
NM_001018004.2(TPM1):c.773-1142A>C
NM_001018004.2(TPM1):c.773-1143del
NM_001018004.2(TPM1):c.773-1148A>C
NM_001018004.2(TPM1):c.773-1150T>G
NM_001018004.2(TPM1):c.773-1155del
NM_001018004.2(TPM1):c.773-1167C>T
NM_001018004.2(TPM1):c.773-1187G>A rs144451403
NM_001018004.2(TPM1):c.773-1188C>T
NM_001018004.2(TPM1):c.773-1191C>T
NM_001018004.2(TPM1):c.773-8C>T
NM_001018005.2(TPM1):c.114+4T>C
NM_001018005.2(TPM1):c.115-192C>T
NM_001018005.2(TPM1):c.115-193A>C
NM_001018005.2(TPM1):c.115-213_115-211delinsTT
NM_001018005.2(TPM1):c.115-214C>G
NM_001018005.2(TPM1):c.115-214_115-211delinsT
NM_001018005.2(TPM1):c.115-226C>T
NM_001018005.2(TPM1):c.115-227G>A
NM_001018005.2(TPM1):c.115-244G>A rs989115520
NM_001018005.2(TPM1):c.115-261C>T rs746952638
NM_001018005.2(TPM1):c.115-266G>A
NM_001018005.2(TPM1):c.115-268G>C
NM_001018005.2(TPM1):c.115-275A>T rs730881132
NM_001018005.2(TPM1):c.115-277G>A
NM_001018005.2(TPM1):c.115-307C>T
NM_001018005.2(TPM1):c.115-316G>A rs397516491
NM_001018005.2(TPM1):c.115-331C>G
NM_001018005.2(TPM1):c.115-334C>T rs1392145197
NM_001018005.2(TPM1):c.115-335G>T rs587780971
NM_001018005.2(TPM1):c.138G>A (p.Leu46=)
NM_001018005.2(TPM1):c.144G>A (p.Lys48=) rs1555403374
NM_001018005.2(TPM1):c.177A>G (p.Lys59=) rs149346709
NM_001018005.2(TPM1):c.234C>A (p.Ala78=)
NM_001018005.2(TPM1):c.241-9T>C rs377417143
NM_001018005.2(TPM1):c.264G>A (p.Leu88=)
NM_001018005.2(TPM1):c.273C>T (p.Arg91=)
NM_001018005.2(TPM1):c.288G>A (p.Glu96=)
NM_001018005.2(TPM1):c.294G>A (p.Glu98=)
NM_001018005.2(TPM1):c.375-5T>C rs377061868
NM_001018005.2(TPM1):c.39C>G (p.Leu13=) rs1439080260
NM_001018005.2(TPM1):c.438C>T (p.Ile146=)
NM_001018005.2(TPM1):c.444G>C (p.Leu148=) rs376518788
NM_001018005.2(TPM1):c.507G>C (p.Leu169=)
NM_001018005.2(TPM1):c.522C>T (p.Ser174=) rs200173919
NM_001018005.2(TPM1):c.549T>C (p.Ala183=) rs199476313
NM_001018005.2(TPM1):c.563+244del
NM_001018005.2(TPM1):c.563+266C>T rs201813515
NM_001018005.2(TPM1):c.563+267G>A rs141757680
NM_001018005.2(TPM1):c.563+284T>C rs1566964956
NM_001018005.2(TPM1):c.563+332A>G rs1566965048
NM_001018005.2(TPM1):c.563+335G>A
NM_001018005.2(TPM1):c.563+337A>C
NM_001018005.2(TPM1):c.563+6C>T
NM_001018005.2(TPM1):c.564-11G>A rs532254032
NM_001018005.2(TPM1):c.564-5A>G rs550286836
NM_001018005.2(TPM1):c.573C>T (p.Ala191=) rs780507307
NM_001018005.2(TPM1):c.585A>G (p.Glu195=)
NM_001018005.2(TPM1):c.627T>G (p.Ala209=)
NM_001018005.2(TPM1):c.640-14C>T
NM_001018005.2(TPM1):c.645G>A (p.Ser215=)
NM_001018005.2(TPM1):c.660A>G (p.Arg220=)
NM_001018005.2(TPM1):c.666G>A (p.Glu222=)
NM_001018005.2(TPM1):c.684T>C (p.Leu228=) rs397516384
NM_001018005.2(TPM1):c.703-12A>T
NM_001018005.2(TPM1):c.703-15A>G
NM_001018005.2(TPM1):c.726G>A (p.Ala242=) rs200484871
NM_001018005.2(TPM1):c.75G>A (p.Ala25=)
NM_001018005.2(TPM1):c.75G>T (p.Ala25=)
NM_001018005.2(TPM1):c.773-3T>C rs113759732
NM_001018005.2(TPM1):c.774C>T (p.Asp258=) rs762282433
NM_001018005.2(TPM1):c.783C>T (p.Tyr261=) rs751001221
NM_001018005.2(TPM1):c.807C>T (p.Ala269=)
NM_001018005.2(TPM1):c.828C>T (p.His276=) rs368813394
NM_001018005.2(TPM1):c.837C>T (p.Asn279=) rs397516393
NM_001018005.2(TPM1):c.840T>C (p.Asp280=)
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser) rs397516395
NM_001018005.2(TPM1):c.851+6C>A rs375043184
NM_001018005.2(TPM1):c.851+6C>T rs375043184
NM_001018005.2(TPM1):c.851+7G>A rs765721221
NM_001018005.2(TPM1):c.852A>T (p.Ile284=)
NM_001018008.2(TPM1):c.*1205T>A
NM_001018008.2(TPM1):c.*1209C>T rs374434837
NM_001018008.2(TPM1):c.*1223C>T rs1057521824
NM_001018008.2(TPM1):c.*1228G>A
NM_001018008.2(TPM1):c.695G>A (p.Arg232His) rs730881128

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