Variant #0000008277 (NC_000001.10:-, LMNA(NM_170707.2):c.29C>T)

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 APS patients have a few overlapping but some distinct clinical features as compared

with HGPS and mandibuloacral dysplasia. The pathogenesis of clinical manifestations in APS pa-

tients seems not to be related to accumulation of mutant farnesylated prelamin A.
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.29C>T - p.Thr10Ile