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

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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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