Variant #0000007970 (NC_000001.10:-, LMNA(NM_170707.2):c.148C>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_00013 See all 3 reported entries
Frequency -
Variant remarks The C148A mutation creates an additional AluI restriction endonuclease site within the exon 1 amplimer, allowing the rapid detection of this mutation in his daughter, who presented at age 24 with isolated quadricep weakness, and at age 28 with atrial and ventricular extrasystoles with no AV block.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNA NM_170707.2 ./. 01 c.148C>A - p.Arg50Ser