Variant #0000008251 (NC_000001.10:-, LMNA(NM_170707.2):c.178C>G)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID LMNA_00009 See all 4 reported entries
Frequency -
Variant remarks The findings demonstrate that the exon 1 c.178 C/G, p.Arg 60 Gly LMNA

gene mutation is associated with a novel phenotype featuring cardiac

involvement followed by late lipodystrophy, diabetes, and peripheral axonal

neuropathy.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNA NM_170707.2 ./. 01 c.178C>G - p.Arg60Gly