Variant #0000007963 (NC_000001.10:-, LMNA(NM_170707.2):c.16C>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_00004 See all 2 reported entries
Frequency -
Variant remarks This transition predicts a

truncated lamin A/C composed of only the five amino-terminal

amino acids. The mutation creates a new BfaI site, which was

used to screen all family members.
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.16C>T - p.Gln6X