ClinVar Miner

List of variants in gene TPM1 reported as uncertain significance by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP
NM_001018005.2(TPM1):c.112C>G (p.Gln38Glu) rs1060501863
NM_001018005.2(TPM1):c.114+3C>T
NM_001018005.2(TPM1):c.115-5C>G rs753196985
NM_001018005.2(TPM1):c.118G>T (p.Glu40Ter) rs104894501
NM_001018005.2(TPM1):c.140A>G (p.Gln47Arg) rs1060501864
NM_001018005.2(TPM1):c.148C>A (p.Leu50Ile) rs1060501866
NM_001018005.2(TPM1):c.148C>T (p.Leu50Phe) rs1060501866
NM_001018005.2(TPM1):c.14_16AGA[2] (p.Lys7del) rs730881155
NM_001018005.2(TPM1):c.152A>G (p.Lys51Arg) rs1566937728
NM_001018005.2(TPM1):c.164A>G (p.Asp55Gly) rs1566937759
NM_001018005.2(TPM1):c.172G>C (p.Asp58His) rs199476304
NM_001018005.2(TPM1):c.209A>C (p.Lys70Thr) rs199476307
NM_001018005.2(TPM1):c.215A>G (p.Glu72Gly)
NM_001018005.2(TPM1):c.226A>G (p.Lys76Glu) rs1555403432
NM_001018005.2(TPM1):c.242C>T (p.Ala81Val)
NM_001018005.2(TPM1):c.253G>A (p.Val85Ile) rs730881156
NM_001018005.2(TPM1):c.253G>T (p.Val85Leu) rs730881156
NM_001018005.2(TPM1):c.262C>G (p.Leu88Val) rs1555407795
NM_001018005.2(TPM1):c.269G>A (p.Arg90Lys)
NM_001018005.2(TPM1):c.377G>T (p.Gly126Val) rs1566962034
NM_001018005.2(TPM1):c.389T>C (p.Ile130Thr) rs727503517
NM_001018005.2(TPM1):c.457C>G (p.His153Asp) rs397516372
NM_001018005.2(TPM1):c.499dup (p.Arg167fs)
NM_001018005.2(TPM1):c.4G>C (p.Asp2His) rs1060501865
NM_001018005.2(TPM1):c.511A>C (p.Ile171Leu) rs774903903
NM_001018005.2(TPM1):c.51C>G (p.Asn17Lys) rs878854150
NM_001018005.2(TPM1):c.538G>C (p.Glu180Gln) rs1555409132
NM_001018005.2(TPM1):c.548C>T (p.Ala183Val) rs397516376
NM_001018005.2(TPM1):c.563+6C>G rs397516378
NM_001018005.2(TPM1):c.572_573delinsTT (p.Ala191Val) rs730881154
NM_001018005.2(TPM1):c.602C>T (p.Thr201Met) rs730881141
NM_001018005.2(TPM1):c.607A>G (p.Asn203Asp) rs1555409523
NM_001018005.2(TPM1):c.625G>T (p.Ala209Ser)
NM_001018005.2(TPM1):c.62G>T (p.Arg21Leu) rs730881151
NM_001018005.2(TPM1):c.713G>T (p.Arg238Leu)
NM_001018005.2(TPM1):c.715G>A (p.Ala239Thr) rs199476318
NM_001018005.2(TPM1):c.736G>A (p.Val246Ile)
NM_001018005.2(TPM1):c.773-3T>C
NM_001018005.2(TPM1):c.784G>A (p.Ala262Thr) rs758506771
NM_001018005.2(TPM1):c.790A>G (p.Lys264Glu) rs397516390
NM_001018005.2(TPM1):c.797A>G (p.Lys266Arg) rs371934474
NM_001018005.2(TPM1):c.806C>T (p.Ala269Val)
NM_001018005.2(TPM1):c.808A>G (p.Ile270Val) rs1555410445
NM_001018005.2(TPM1):c.814G>A (p.Glu272Lys)
NM_001018005.2(TPM1):c.82G>C (p.Asp28His) rs397516391
NM_001018005.2(TPM1):c.841A>G (p.Met281Val) rs397516394
NM_001018005.2(TPM1):c.850A>G (p.Ile284Val) rs199476322
NM_001018005.2(TPM1):c.851+6C>A rs375043184
NM_001018005.2(TPM1):c.851+6C>T rs375043184
NM_001018005.2(TPM1):c.88_89delinsGC (p.Lys30Ala) rs1555402999
NM_001018005.2(TPM1):c.98A>C (p.Glu33Ala) rs886039444

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.