Variant #0000008369 (NC_000001.10:-, LMNA(NM_170707.2):c.73C>G)

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_00101 See all 4 reported entries
Frequency -
Variant remarks The mutation R25G in exon 1 of LMNA gene we reported here in a Chinese family had a phenotype of

malignant arrhythmia and mild LGMD, suggesting that patients with familial DCM, conduction system defects and skeletal

muscle dystrophy should be screened by genetic testing for the LMNA gene
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.73C>G - p.Arg25Gly