Annotation Detail
Information
- Associated Genes
- TNNT2
- Associated Variants
-
TNNT2 p.Arg151= (p.R151=)
(
ENST00000367320.6,
ENST00000367322.6,
ENST00000658476.1,
ENST00000422165.6,
ENST00000509001.5,
ENST00000455702.7,
ENST00000714317.1,
ENST00000660295.1,
ENST00000656932.1,
ENST00000412633.3,
ENST00000438742.6,
ENST00000367318.10,
ENST00000714316.2,
ENST00000714312.1,
ENST00000714313.1,
ENST00000714314.1 )
TNNT2 p.Arg151= (p.R151=) ( ENST00000367318.10, ENST00000367320.6, ENST00000367322.6, ENST00000412633.3, ENST00000422165.6, ENST00000438742.6, ENST00000455702.7, ENST00000509001.5, ENST00000656932.1, ENST00000658476.1, ENST00000660295.1, ENST00000714312.1, ENST00000714313.1, ENST00000714314.1, ENST00000714316.2, ENST00000714317.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) AND not specified
- ClinVar Allele ID
- 52812
- ClinVar RefSeq Alternation Syntax
- NM_001276345.2:c.451C>A
- ClinVar RefSeq Alternation Syntax
- NM_000364.4:c.451C>A
- ClinVar RefSeq Alternation Syntax
- NM_001276346.2:c.331C>A
- ClinVar RefSeq Alternation Syntax
- NM_001276347.2:c.421C>A
- ClinVar RefSeq Alternation Syntax
- NM_001001430.3:c.421C>A
- ClinVar RefSeq Alternation Syntax
- NM_001001431.3:c.421C>A
- ClinVar RefSeq Alternation Syntax
- NM_001001432.3:c.406C>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2012-01-06
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000036591
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs