ClinVar Miner

List of variants in gene TNNC1 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003280.3(TNNC1):c.203-5C>T rs142519988 0.00151
NM_003280.3(TNNC1):c.201C>T (p.Asp67=) rs150881554 0.00074
NM_003280.3(TNNC1):c.108C>A (p.Ile36=) rs202000367 0.00030
NM_003280.3(TNNC1):c.324T>C (p.Ala108=) rs145066209 0.00019
NM_003280.3(TNNC1):c.210C>T (p.Gly70=) rs141505676 0.00010
NM_003280.3(TNNC1):c.435C>A (p.Asp145Glu) rs267607124 0.00010
NM_003280.3(TNNC1):c.207C>T (p.Ser69=) rs202173903 0.00004
NM_003280.3(TNNC1):c.317+9G>A rs761287435 0.00004
NM_003280.3(TNNC1):c.24+13G>T rs748590123 0.00003
NM_003280.3(TNNC1):c.288G>A (p.Glu96=) rs200066743 0.00003
NM_003280.3(TNNC1):c.203-10C>G rs727505237 0.00002
NM_003280.3(TNNC1):c.56-8G>A rs727503495 0.00002
NM_003280.3(TNNC1):c.144G>T (p.Leu48=) rs1251887019 0.00001
NM_003280.3(TNNC1):c.203-16T>C rs765306660 0.00001
NM_003280.3(TNNC1):c.23C>T (p.Ala8Val) rs267607125 0.00001
NM_003280.3(TNNC1):c.402G>T (p.Glu134Asp) rs397516847 0.00001
NM_003280.3(TNNC1):c.442A>G (p.Ile148Val) rs397516848 0.00001
NM_003280.3(TNNC1):c.454+6C>G rs750021293 0.00001
NM_003280.3(TNNC1):c.456G>A (p.Glu152=) rs568828576 0.00001
NM_003280.3(TNNC1):c.56-9T>C rs727503497 0.00001
NM_003280.3(TNNC1):c.86T>A (p.Leu29Gln) rs267607123 0.00001
NM_003280.3(TNNC1):c.90C>T (p.Gly30=) rs149647795 0.00001
NM_003280.3(TNNC1):c.-7C>A
NM_003280.3(TNNC1):c.102C>A (p.Gly34=) rs1048914110
NM_003280.3(TNNC1):c.153C>A (p.Asn51Lys) rs1057518507
NM_003280.3(TNNC1):c.157A>G (p.Thr53Ala) rs1553651742
NM_003280.3(TNNC1):c.161C>A (p.Pro54His) rs876661393
NM_003280.3(TNNC1):c.203-14C>T
NM_003280.3(TNNC1):c.24+1G>A rs727503498
NM_003280.3(TNNC1):c.24+6G>A rs1057521396
NM_003280.3(TNNC1):c.285G>T (p.Glu95Asp) rs2153229927
NM_003280.3(TNNC1):c.317+6C>G rs2153229925
NM_003280.3(TNNC1):c.387G>C (p.Thr129=) rs397516845
NM_003280.3(TNNC1):c.394G>A (p.Asp132Asn) rs397516846
NM_003280.3(TNNC1):c.427AAC[1] (p.Asn144del) rs1553651630
NM_003280.3(TNNC1):c.431A>G (p.Asn144Ser) rs750978833
NM_003280.3(TNNC1):c.435C>T (p.Asp145=) rs267607124
NM_003280.3(TNNC1):c.445G>A (p.Asp149Asn) rs397516849
NM_003280.3(TNNC1):c.454+16G>A
NM_003280.3(TNNC1):c.454+6C>T rs750021293
NM_003280.3(TNNC1):c.455-14C>A rs587780966
NM_003280.3(TNNC1):c.480G>A (p.Val160=) rs727504896
NM_003280.3(TNNC1):c.5A>G (p.Asp2Gly) rs397516850
NM_003280.3(TNNC1):c.74_82del (p.Asp25_Phe27del) rs727503496
NM_003280.3(TNNC1):c.97G>A (p.Asp33Asn) rs727503494

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.