Variant #0000008396 (NC_000001.10:-, LMNA(NM_170707.2):c.?)

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_00087
Frequency -
Variant remarks The

presence of short inverted sequence homologies at the breakpoint junctions suggested a mutational event involving serial

replication slippage in trans during DNA replication.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNA NM_170707.2 ./. 00 c.? - p.?