List of variants in gene TNNC1 reported by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 69

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.393C>T (p.Asp131=)	rs147821122	0.00010
NM_003280.3(TNNC1):c.435C>A (p.Asp145Glu)	rs267607124	0.00010
NM_003280.3(TNNC1):c.195C>T (p.Asp65=)	rs370426309	0.00006
NM_003280.3(TNNC1):c.444C>T (p.Ile148=)	rs149428762	0.00006
NM_003280.3(TNNC1):c.105C>T (p.Cys35=)	rs1359525416	0.00004
NM_003280.3(TNNC1):c.207C>T (p.Ser69=)	rs202173903	0.00004
NM_003280.3(TNNC1):c.183C>T (p.Ile61=)	rs764114178	0.00003
NM_003280.3(TNNC1):c.432C>T (p.Asn144=)	rs767979684	0.00003
NM_003280.3(TNNC1):c.474G>A (p.Lys158=)	rs770807038	0.00003
NM_003280.3(TNNC1):c.72C>T (p.Phe24=)	rs751682878	0.00003
NM_003280.3(TNNC1):c.216G>A (p.Val72=)	rs770331194	0.00002
NM_003280.3(TNNC1):c.243G>C (p.Met81Ile)	rs545564444	0.00002
NM_003280.3(TNNC1):c.180G>A (p.Met60Ile)	rs1471808574	0.00001
NM_003280.3(TNNC1):c.202+5G>C	rs759472560	0.00001
NM_003280.3(TNNC1):c.208G>A (p.Gly70Ser)	rs772752716	0.00001
NM_003280.3(TNNC1):c.222T>C (p.Phe74=)	rs746394204	0.00001
NM_003280.3(TNNC1):c.23C>T (p.Ala8Val)	rs267607125	0.00001
NM_003280.3(TNNC1):c.242T>C (p.Met81Thr)	rs771216638	0.00001
NM_003280.3(TNNC1):c.304C>T (p.Arg102Cys)	rs370103102	0.00001
NM_003280.3(TNNC1):c.305G>A (p.Arg102His)	rs143020831	0.00001
NM_003280.3(TNNC1):c.327T>C (p.Asp109=)	rs1191773624	0.00001
NM_003280.3(TNNC1):c.386C>T (p.Thr129Met)	rs749367654	0.00001
NM_003280.3(TNNC1):c.402G>T (p.Glu134Asp)	rs397516847	0.00001
NM_003280.3(TNNC1):c.418G>A (p.Gly140Arg)	rs752100917	0.00001
NM_003280.3(TNNC1):c.419G>A (p.Gly140Glu)	rs764835690	0.00001
NM_003280.3(TNNC1):c.430A>G (p.Asn144Asp)	rs730881061	0.00001
NM_003280.3(TNNC1):c.436G>A (p.Gly146Ser)	rs567327895	0.00001
NM_003280.3(TNNC1):c.469A>C (p.Met157Leu)	rs730880230	0.00001
NM_003280.3(TNNC1):c.90C>T (p.Gly30=)	rs149647795	0.00001
NM_003280.3(TNNC1):c.102C>A (p.Gly34=)	rs1048914110
NM_003280.3(TNNC1):c.116A>G (p.Lys39Arg)
NM_003280.3(TNNC1):c.123G>T (p.Leu41=)
NM_003280.3(TNNC1):c.154C>T (p.Pro52Ser)
NM_003280.3(TNNC1):c.155C>G (p.Pro52Arg)	rs730881065
NM_003280.3(TNNC1):c.158C>A (p.Thr53Asn)
NM_003280.3(TNNC1):c.168G>A (p.Glu56=)
NM_003280.3(TNNC1):c.17A>G (p.Lys6Arg)	rs2153230085
NM_003280.3(TNNC1):c.184G>A (p.Asp62Asn)	rs1040079072
NM_003280.3(TNNC1):c.212C>T (p.Thr71Met)	rs1706331809
NM_003280.3(TNNC1):c.213G>A (p.Thr71=)	rs140287760
NM_003280.3(TNNC1):c.225T>G (p.Asp75Glu)
NM_003280.3(TNNC1):c.230del (p.Phe77fs)
NM_003280.3(TNNC1):c.241A>T (p.Met81Leu)
NM_003280.3(TNNC1):c.25G>A (p.Val9Ile)	rs1578264552
NM_003280.3(TNNC1):c.341T>G (p.Leu114Arg)	rs2153229918
NM_003280.3(TNNC1):c.363G>T (p.Leu121=)
NM_003280.3(TNNC1):c.375C>T (p.Gly125=)
NM_003280.3(TNNC1):c.387G>C (p.Thr129=)	rs397516845
NM_003280.3(TNNC1):c.400G>A (p.Glu134Lys)	rs1553651640
NM_003280.3(TNNC1):c.402G>A (p.Glu134=)
NM_003280.3(TNNC1):c.412A>G (p.Lys138Glu)
NM_003280.3(TNNC1):c.416A>G (p.Asp139Gly)
NM_003280.3(TNNC1):c.417C>T (p.Asp139=)	rs757904305
NM_003280.3(TNNC1):c.424_425del (p.Lys142fs)
NM_003280.3(TNNC1):c.435C>T (p.Asp145=)	rs267607124
NM_003280.3(TNNC1):c.440G>A (p.Arg147His)	rs769919235
NM_003280.3(TNNC1):c.444C>A (p.Ile148=)
NM_003280.3(TNNC1):c.456G>C (p.Glu152Asp)	rs568828576
NM_003280.3(TNNC1):c.53A>C (p.Asn18Thr)
NM_003280.3(TNNC1):c.57G>T (p.Glu19Asp)
NM_003280.3(TNNC1):c.5A>G (p.Asp2Gly)	rs397516850
NM_003280.3(TNNC1):c.65C>T (p.Ala22Val)
NM_003280.3(TNNC1):c.93T>C (p.Ala31=)	rs1578264358
NM_003280.3(TNNC1):c.94G>A (p.Glu32Lys)	rs1553651750

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.