Variant #0000008133 (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 These patients extend the spectrum of abnormal

phenotypes caused by LMNA mutations, which may

complicate the clinical diagnosis of some patients with

laminopathies, but suggest that LMNA is a good

candidate for evaluation in patients with other atypical

progeria phenotypes
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