Variant #0000000667 (NC_000001.10:g.156104674C>T, NM_170707.3:c.718C>T (LMNA))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.156104674C>T
Reference -
DB-ID LMNA_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2025-10-06 06:18:45 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
LMNA NM_170707.3 +?/+? - c.718C>T r.(?) p.(Arg240Trp) likely pathogenic