Variant #0000008252 (NC_000001.10:-, LMNA(NM_170707.2):c.777T>A)

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_00113 See all 6 reported entries
Frequency -
Variant remarks the present report demonstrates for the first

time the essential role of lamins A and C in human fibroblasts

and identifies the molecular and cellular events leading

to NE disorganization, which represents the first step

toward the disease.
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 ./. 04 c.777T>A - p.Tyr259X