Annotation Detail

Information
Associated Genes
TNNT2
Associated Variants
TNNT2 c.851+1G>A ( ENST00000714316.2, ENST00000438742.6, ENST00000367318.10, ENST00000714313.1, ENST00000714314.1, ENST00000714312.1, ENST00000422165.6, ENST00000509001.5, ENST00000658476.1, ENST00000367322.6, ENST00000367320.6, ENST00000412633.3, ENST00000656932.1, ENST00000455702.7, ENST00000714317.1, ENST00000660295.1 )
TNNT2 c.851+1G>A ( 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
hypertrophic cardiomyopathy
Source Database
ClinVar
Description
NM_001276345.2(TNNT2):c.851+1G>A AND Hypertrophic cardiomyopathy
ClinVar Allele ID
52842
ClinVar RefSeq Alternation Syntax
NM_001276347.2:c.821+1G>A
ClinVar RefSeq Alternation Syntax
NM_001001431.3:c.812+1G>A
ClinVar RefSeq Alternation Syntax
NM_001406727.1:c.812+1G>A
ClinVar RefSeq Alternation Syntax
NM_000364.4:c.842+1G>A
ClinVar RefSeq Alternation Syntax
NM_001406724.1:c.821+1G>A
ClinVar RefSeq Alternation Syntax
NM_001276345.2:c.851+1G>A
ClinVar RefSeq Alternation Syntax
NM_001001432.3:c.803+1G>A
ClinVar RefSeq Alternation Syntax
NM_001001430.3:c.821+1G>A
ClinVar RefSeq Alternation Syntax
NM_001276346.2:c.722+1G>A
ClinVar RefSeq Alternation Syntax
NM_001406725.1:c.818+1G>A
ClinVar RefSeq Alternation Syntax
NM_001406726.1:c.812+1G>A
ClinVar RefSeq Alternation Syntax
NM_001406723.1:c.842+1G>A
ClinVar RefSeq Alternation Syntax
NM_001406728.1:c.806+1G>A
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2014-12-22
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000036621
ClinVar Disease
Hypertrophic cardiomyopathy
Observed Origin Sample
germline
Drugs