Variant #0000008002 (NC_000001.10:-, LMNA(NM_170707.2):c.28_29insA)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Insertion
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID LMNA_00053
Frequency -
Variant remarks This is a previously described (R377H) mutation in another family with a quadriceps myopathy associated with DCM.
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.28_29insA - p.Thr10AsnfsX31