chr1:156104740:G>T Detail (hg19) (LMNA)

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

Genome

Assembly	Position
hg19	chr1:156,104,740-156,104,740
hg38	chr1:156,134,949-156,134,949 View the variant detail on this assembly version.

HGVS

LMNA

Type	Transcript	Protein
RefSeq	NM_001282625.1:c.784G>T	NP_001269554.1:p.Glu262Ter
	NM_005572.3:c.784G>T	NP_005563.1:p.Glu262Ter
	NM_001282624.1:c.541G>T	NP_001269553.1:p.Glu181Ter
	NM_001282626.1:c.784G>T	NP_001269555.1:p.Glu262Ter
	NM_170707.3:c.784G>T	NP_733821.1:p.Glu262Ter
	NM_001257374.2:c.448G>T	NP_001244303.1:p.Glu150Ter
Ensemble	ENST00000368301.6:c.784G>T	ENST00000368301.6:p.Glu262Ter
	ENST00000677389.1:c.784G>T	ENST00000677389.1:p.Glu262Ter
	ENST00000675667.1:c.784G>T	ENST00000675667.1:p.Glu262Ter
	ENST00000675939.1:c.784G>T	ENST00000675939.1:p.Glu262Ter
	ENST00000368297.5:c.541G>T	ENST00000368297.5:p.Glu181Ter
	ENST00000683032.1:c.784G>T	ENST00000683032.1:p.Glu262Ter
	ENST00000473598.6:c.487G>T	ENST00000473598.6:p.Glu163Ter
	ENST00000368299.7:c.784G>T	ENST00000368299.7:p.Glu262Ter
	ENST00000361308.9:c.784G>T	ENST00000361308.9:p.Glu262Ter
	ENST00000368300.9:c.784G>T	ENST00000368300.9:p.Glu262Ter
	ENST00000682650.1:c.784G>T	ENST00000682650.1:p.Glu262Ter
	ENST00000504687.7:c.226G>T	ENST00000504687.7:p.Glu76Ter
	ENST00000676385.2:c.784G>T	ENST00000676385.2:p.Glu262Ter
	ENST00000448611.6:c.448G>T	ENST00000448611.6:p.Glu150Ter

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic Likely pathogenic
Review star
Show details

Links

LMNA

Type	Database	ID	Link
Gene	MIM	150330	OMIM
	HGNC	6636	HGNC
	Ensembl	ENSG00000160789	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	2012-09-26	criteria provided, single submitter	Primary dilated cardiomyopathy	germline	Detail
Pathogenic	2023-07-19	criteria provided, single submitter	Charcot-Marie-Tooth disease type 2	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.443	Cardiomyopathy, Familial Idiopathic	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_170707.4(LMNA):c.784G>T (p.Glu262Ter) AND Primary dilated cardiomyopathy	ClinVar	Detail
NM_170707.4(LMNA):c.784G>T (p.Glu262Ter) AND Charcot-Marie-Tooth disease type 2	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: rs397517909 dbSNP
Genome: hg19
Position: chr1:156,104,740-156,104,740
Variant Type: snv
Reference Allele: G
Alternative Allele: T

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