chr1:156136110:C>T 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	chr1:156,105,901-156,105,901 View the variant detail on this assembly version.
hg38	chr1:156,136,110-156,136,110

HGVS

LMNA

Type	Transcript	Protein
RefSeq	NM_001282624.1:c.903C>T	NP_001269553.1:p.Gly301=
	NM_001282626.1:c.1146C>T	NP_001269555.1:p.Gly382=
	NM_170707.3:c.1146C>T	NP_733821.1:p.Gly382=
	NM_001282625.1:c.1146C>T	NP_001269554.1:p.Gly382=
	NM_005572.3:c.1146C>T	NP_005563.1:p.Gly382=
	NM_001257374.2:c.810C>T	NP_001244303.1:p.Gly270=
Ensemble	ENST00000361308.9:c.1146C>T	ENST00000361308.9:p.Gly382=
	ENST00000368297.5:c.903C>T	ENST00000368297.5:p.Gly301=
	ENST00000368299.7:c.1146C>T	ENST00000368299.7:p.Gly382=
	ENST00000368300.9:c.1146C>T	ENST00000368300.9:p.Gly382=
	ENST00000368301.6:c.1146C>T	ENST00000368301.6:p.Gly382=
	ENST00000448611.6:c.810C>T	ENST00000448611.6:p.Gly270=
	ENST00000473598.6:c.849C>T	ENST00000473598.6:p.Gly283=
	ENST00000504687.7:c.588C>T	ENST00000504687.7:p.Gly196=
	ENST00000675667.1:c.1146C>T	ENST00000675667.1:p.Gly382=
	ENST00000675939.1:c.1146C>T	ENST00000675939.1:p.Gly382=
	ENST00000676385.2:c.1146C>T	ENST00000676385.2:p.Gly382=
	ENST00000677389.1:c.1146C>T	ENST00000677389.1:p.Gly382=
	ENST00000682650.1:c.1146C>T	ENST00000682650.1:p.Gly382=
	ENST00000683032.1:c.1146C>T	ENST00000683032.1:p.Gly382=

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	tgv242733284	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely pathogenic	2018-05-25	criteria provided, single submitter	neuromuscular disease,Primary dilated cardiomyopathy	germline	Detail
Likely pathogenic	2018-05-25	criteria provided, single submitter	neuromuscular disease,Primary dilated cardiomyopathy	germline	Detail
Pathogenic Likely pathogenic	2024-04-01	criteria provided, multiple submitters, no conflicts	not provided	germline not provided	Detail
Pathogenic	2024-01-27	criteria provided, single submitter	Charcot-Marie-Tooth disease type 2	germline	Detail
Likely pathogenic	2021-03-08	criteria provided, single submitter		germline	Detail
Likely pathogenic	2021-04-27	no assertion criteria provided	dilated cardiomyopathy 1A	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.1146C>T (p.Gly382=) AND multiple conditions	ClinVar	Detail
NM_170707.4(LMNA):c.1146C>T (p.Gly382=) AND multiple conditions	ClinVar	Detail
NM_170707.4(LMNA):c.1146C>T (p.Gly382=) AND not provided	ClinVar	Detail
NM_170707.4(LMNA):c.1146C>T (p.Gly382=) AND Charcot-Marie-Tooth disease type 2	ClinVar	Detail
NM_170707.4(LMNA):c.1146C>T (p.Gly382=) AND Cardiovascular phenotype	ClinVar	Detail
NM_170707.4(LMNA):c.1146C>T (p.Gly382=) AND Dilated cardiomyopathy 1A	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: rs57508089 dbSNP
Genome: hg38
Position: chr1:156,136,110-156,136,110
Variant Type: snv
Reference Allele: C
Alternative Allele: T

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