chr1:156136952:G>A Detail (hg38) (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	chr1:156,106,743-156,106,743 View the variant detail on this assembly version.
hg38	chr1:156,136,952-156,136,952

HGVS

LMNA

Type	Transcript	Protein
RefSeq	NM_001282624.1:c.1169G>A	NP_001269553.1:p.Arg390His
	NM_001282626.1:c.1412G>A	NP_001269555.1:p.Arg471His
	NM_170707.3:c.1412G>A	NP_733821.1:p.Arg471His
	NM_001282625.1:c.1412G>A	NP_001269554.1:p.Arg471His
	NM_005572.3:c.1412G>A	NP_005563.1:p.Arg471His
	NM_001257374.2:c.1076G>A	NP_001244303.1:p.Arg359His
Ensemble	ENST00000361308.9:c.1412G>A	ENST00000361308.9:p.Arg471His
	ENST00000368297.5:c.1169G>A	ENST00000368297.5:p.Arg390His
	ENST00000368299.7:c.1412G>A	ENST00000368299.7:p.Arg471His
	ENST00000368300.9:c.1412G>A	ENST00000368300.9:p.Arg471His
	ENST00000368301.6:c.1412G>A	ENST00000368301.6:p.Arg471His
	ENST00000448611.6:c.1076G>A	ENST00000448611.6:p.Arg359His
	ENST00000473598.6:c.1115G>A	ENST00000473598.6:p.Arg372His
	ENST00000504687.7:c.854G>A	ENST00000504687.7:p.Arg285His
	ENST00000675667.1:c.1412G>A	ENST00000675667.1:p.Arg471His
	ENST00000675939.1:c.1412G>A	ENST00000675939.1:p.Arg471His
	ENST00000676385.2:c.1412G>A	ENST00000676385.2:p.Arg471His
	ENST00000677389.1:c.1412G>A	ENST00000677389.1:p.Arg471His
	ENST00000682650.1:c.1412G>A	ENST00000682650.1:p.Arg471His
	ENST00000683032.1:c.1412G>A	ENST00000683032.1:p.Arg471His

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	COSM4023184	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2023-10-02	criteria provided, multiple submitters, no conflicts	Primary dilated cardiomyopathy	germline	Detail
Pathogenic Likely pathogenic	2023-06-09	criteria provided, multiple submitters, no conflicts	not provided	germline not provided	Detail
Pathogenic Likely pathogenic	2023-02-23	criteria provided, multiple submitters, no conflicts	dilated cardiomyopathy 1A	germline unknown	Detail
Pathogenic	2023-03-13	criteria provided, single submitter		germline	Detail
Pathogenic	2024-01-06	criteria provided, single submitter	Charcot-Marie-Tooth disease type 2	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.298	Cardiomyopathy, Dilated	The presumed pathogenic mutations were distributed with one case of suspected HC...	BeFree	22177269	Detail
0.262	Cardiomyopathy, Dilated	The presumed pathogenic mutations were distributed with one case of suspected HC...	BeFree	22177269	Detail
0.298	Cardiomyopathy, Dilated	NA	CLINVAR		Detail
0.443	Cardiomyopathy, Familial Idiopathic	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_170707.4(LMNA):c.1412G>A (p.Arg471His) AND Primary dilated cardiomyopathy	ClinVar	Detail
NM_170707.4(LMNA):c.1412G>A (p.Arg471His) AND not provided	ClinVar	Detail
NM_170707.4(LMNA):c.1412G>A (p.Arg471His) AND Dilated cardiomyopathy 1A	ClinVar	Detail
NM_170707.4(LMNA):c.1412G>A (p.Arg471His) AND Cardiovascular phenotype	ClinVar	Detail
NM_170707.4(LMNA):c.1412G>A (p.Arg471His) AND Charcot-Marie-Tooth disease type 2	ClinVar	Detail
The presumed pathogenic mutations were distributed with one case of suspected HCM and DCM (MYH7; p.R...	DisGeNET	Detail
The presumed pathogenic mutations were distributed with one case of suspected HCM and DCM (MYH7; p.R...	DisGeNET	Detail
NA	DisGeNET	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: rs267607578 dbSNP
Genome: hg38
Position: chr1:156,136,952-156,136,952
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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