chr1:156136934: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	chr1:156,106,725-156,106,725 View the variant detail on this assembly version.
hg38	chr1:156,136,934-156,136,934

HGVS

LMNA

Type	Transcript	Protein
RefSeq	NM_001282624.1:c.1151G>A	NP_001269553.1:p.Gly384Asp
	NM_001282626.1:c.1394G>A	NP_001269555.1:p.Gly465Asp
	NM_170707.3:c.1394G>A	NP_733821.1:p.Gly465Asp
	NM_001282625.1:c.1394G>A	NP_001269554.1:p.Gly465Asp
	NM_005572.3:c.1394G>A	NP_005563.1:p.Gly465Asp
	NM_001257374.2:c.1058G>A	NP_001244303.1:p.Gly353Asp
Ensemble	ENST00000361308.9:c.1394G>A	ENST00000361308.9:p.Gly465Asp
	ENST00000368297.5:c.1151G>A	ENST00000368297.5:p.Gly384Asp
	ENST00000368299.7:c.1394G>A	ENST00000368299.7:p.Gly465Asp
	ENST00000368300.9:c.1394G>A	ENST00000368300.9:p.Gly465Asp
	ENST00000368301.6:c.1394G>A	ENST00000368301.6:p.Gly465Asp
	ENST00000448611.6:c.1058G>A	ENST00000448611.6:p.Gly353Asp
	ENST00000473598.6:c.1097G>A	ENST00000473598.6:p.Gly366Asp
	ENST00000504687.7:c.836G>A	ENST00000504687.7:p.Gly279Asp
	ENST00000675667.1:c.1394G>A	ENST00000675667.1:p.Gly465Asp
	ENST00000675939.1:c.1394G>A	ENST00000675939.1:p.Gly465Asp
	ENST00000676385.2:c.1394G>A	ENST00000676385.2:p.Gly465Asp
	ENST00000677389.1:c.1394G>A	ENST00000677389.1:p.Gly465Asp
	ENST00000682650.1:c.1394G>A	ENST00000682650.1:p.Gly465Asp
	ENST00000683032.1:c.1394G>A	ENST00000683032.1:p.Gly465Asp

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
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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
Pathogenic	2016-01-22	criteria provided, single submitter	Familial partial lipodystrophy, Dunnigan type	germline	Detail
not provided		no assertion provided	not provided	not provided	Detail
Likely pathogenic	2022-11-29	criteria provided, single submitter	Charcot-Marie-Tooth disease type 2	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.362	Familial Partial Lipodystrophy, Type 2	NA	CLINVAR		Detail
0.627	progeria	The mutant constructs used included the laminopathy-inducing lamin A rod domain ...	BeFree	16440304	Detail

Annotation

Annotations

Descrption	Source	Links
NM_170707.4(LMNA):c.1394G>A (p.Gly465Asp) AND Familial partial lipodystrophy, Dunnigan type	ClinVar	Detail
NM_170707.4(LMNA):c.1394G>A (p.Gly465Asp) AND not provided	ClinVar	Detail
NM_170707.4(LMNA):c.1394G>A (p.Gly465Asp) AND Charcot-Marie-Tooth disease type 2	ClinVar	Detail
NA	DisGeNET	Detail
The mutant constructs used included the laminopathy-inducing lamin A rod domain mutants N195K, E358K...	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: rs61282106 dbSNP
Genome: hg38
Position: chr1:156,136,934-156,136,934
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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