Annotation Detail
Information
- Associated Genes
- TNNC1
- Associated Variants
-
TNNC1 p.Asp145= (p.D145=)
(
ENST00000232975.8 )
TNNC1 p.Asp145Glu (p.D145E) ( ENST00000232975.8 )
TNNC1 p.Asp145Glu (p.D145E) ( ENST00000232975.8 )
TNNC1 p.Cys84Tyr (p.C84Y) ( ENST00000232975.8 )
TNNC1 p.Ala31Ser (p.A31S) ( ENST00000232975.8 )
TNNC1 p.Ala31Thr (p.A31T) ( ENST00000232975.8 )
TNNC1 p.Leu29Gln (p.L29Q) ( ENST00000232975.8 )
TNNC1 p.Ala8Val (p.A8V) ( ENST00000232975.8 )
TNNC1 p.Asp145= (p.D145=) ( ENST00000232975.8 )
TNNC1 p.Asp145Glu (p.D145E) ( ENST00000232975.8 )
TNNC1 p.Asp145Glu (p.D145E) ( ENST00000232975.8 )
TNNC1 p.Cys84Tyr (p.C84Y) ( ENST00000232975.8 )
TNNC1 p.Ala31Ser (p.A31S) ( ENST00000232975.8 )
TNNC1 p.Ala31Thr (p.A31T) ( ENST00000232975.8 )
TNNC1 p.Leu29Gln (p.L29Q) ( ENST00000232975.8 )
TNNC1 p.Ala8Val (p.A8V) ( ENST00000232975.8 ) - Associated Disease
- Cardiomyopathy, Familial Hypertrophic, 13
- Source Database
- DisGeNET
- Description
- NA
- Original source reporting the Gene Disease association
- CLINVAR
- DisGENET score for the Gene Disease association
- 0.36
- Year of publication
- NA
Drugs