chr1:156115066: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	chr1:156,084,857-156,084,857 View the variant detail on this assembly version.
hg38	chr1:156,115,066-156,115,066

HGVS

LMNA

Type	Transcript	Protein
RefSeq	NM_001282626.1:c.148C>T	NP_001269555.1:p.Arg50Cys
	NM_170707.3:c.148C>T	NP_733821.1:p.Arg50Cys
	NM_001282625.1:c.148C>T	NP_001269554.1:p.Arg50Cys
	NM_005572.3:c.148C>T	NP_005563.1:p.Arg50Cys
Ensemble	ENST00000361308.9:c.148C>T	ENST00000361308.9:p.Arg50Cys
	ENST00000368299.7:c.148C>T	ENST00000368299.7:p.Arg50Cys
	ENST00000368300.9:c.148C>T	ENST00000368300.9:p.Arg50Cys
	ENST00000368301.6:c.148C>T	ENST00000368301.6:p.Arg50Cys
	ENST00000675667.1:c.148C>T	ENST00000675667.1:p.Arg50Cys
	ENST00000675939.1:c.148C>T	ENST00000675939.1:p.Arg50Cys
	ENST00000676385.2:c.148C>T	ENST00000676385.2:p.Arg50Cys
	ENST00000677389.1:c.148C>T	ENST00000677389.1:p.Arg50Cys
	ENST00000682650.1:c.148C>T	ENST00000682650.1:p.Arg50Cys
	ENST00000683032.1:c.148C>T	ENST00000683032.1:p.Arg50Cys

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Conflicting classifications of pathogenicity
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
Uncertain significance	2013-11-12	criteria provided, single submitter	not provided	germline	Detail
Pathogenic	2024-03-17	criteria provided, single submitter	congenital muscular dystrophy due to LMNA mutation	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.447	Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)	Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscu...	UNIPROT	11503164	Detail

Annotation

Annotations

Descrption	Source	Links
NM_170707.4(LMNA):c.148C>T (p.Arg50Cys) AND not provided	ClinVar	Detail
NM_170707.4(LMNA):c.148C>T (p.Arg50Cys) AND Congenital muscular dystrophy due to LMNA mutation	ClinVar	Detail
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.	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: rs59931416 dbSNP
Genome: hg38
Position: chr1:156,115,066-156,115,066
Variant Type: snv
Reference Allele: C
Alternative Allele: T

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