chr1:201365610:A>C Detail (hg38) (TNNT2)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr1:201,334,738-201,334,738 View the variant detail on this assembly version.
hg38	chr1:201,365,610-201,365,610

HGVS

TNNT2

Type	Transcript	Protein
RefSeq	NM_001001430.2:c.264T>G	NP_001001430.1:p.Asp88Glu
	NM_001276346.1:c.291T>G	NP_001263275.1:p.Asp97Glu
	NM_001001431.2:c.261T>G	NP_001001431.1:p.Asp87Glu
	NM_001276347.1:c.264T>G	NP_001263276.1:p.Asp88Glu
Ensemble	ENST00000367318.10:c.264T>G	ENST00000367318.10:p.Asp88Glu
	ENST00000367320.6:c.291T>G	ENST00000367320.6:p.Asp97Glu
	ENST00000367322.6:c.261T>G	ENST00000367322.6:p.Asp87Glu
	ENST00000412633.3:c.264T>G	ENST00000412633.3:p.Asp88Glu
	ENST00000422165.6:c.294T>G	ENST00000422165.6:p.Asp98Glu
	ENST00000438742.6:c.246T>G	ENST00000438742.6:p.Asp82Glu
	ENST00000455702.7:c.279T>G	ENST00000455702.7:p.Asp93Glu
	ENST00000509001.5:c.264T>G	ENST00000509001.5:p.Asp88Glu
	ENST00000656932.1:c.294T>G	ENST00000656932.1:p.Asp98Glu
	ENST00000658476.1:c.264T>G	ENST00000658476.1:p.Asp88Glu
	ENST00000660295.1:c.264T>G	ENST00000660295.1:p.Asp88Glu
	ENST00000714312.1:c.87T>G	ENST00000714312.1:p.Asp29Glu
	ENST00000714313.1:c.249T>G	ENST00000714313.1:p.Asp83Glu
	ENST00000714314.1:c.294T>G	ENST00000714314.1:p.Asp98Glu
	ENST00000714316.2:c.264T>G	ENST00000714316.2:p.Asp88Glu
	ENST00000714317.1:c.87T>G	ENST00000714317.1:p.Asp29Glu

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Likely pathogenic
Review star
Show details

Links

TNNT2

Type	Database	ID	Link
Gene	MIM	191045	OMIM
	HGNC	11949	HGNC
	Ensembl	ENSG00000118194	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2015-06-04	criteria provided, single submitter	Primary dilated cardiomyopathy	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.440	CARDIOMYOPATHY, DILATED, 1D (disorder)	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_001276345.2(TNNT2):c.294T>G (p.Asp98Glu) AND Primary dilated cardiomyopathy	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs397516454 dbSNP
Genome: hg38
Position: chr1:201,365,610-201,365,610
Variant Type: snv
Reference Allele: A
Alternative Allele: C

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