Variant #0000008336 (NC_000001.10:-, LMNA(NM_170707.2):c.1868C>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_00204 See all 3 reported entries
Frequency -
Variant remarks The LMNA c.1868C>G (p.T623S) mutation either

leads to the substitution of a serine to a threonine or activates a cryptic splice site, producing a protein

product that truncates 35 amino acids
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 ./. 11 c.1868C>G - p.Thr623Ser