Variant #0000928042 (NC_000001.10:g.156106775C>T, NM_170707.3:c.1444C>T (LMNA))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.156106775C>T
DNA change (hg38) -
Published as LMNA(NM_170707.2):c.1444C>T (p.R482W), LMNA(NM_170707.3):c.1444C>T (p.(Arg482Trp))
ISCN -
DB-ID LMNA_000011 See all 24 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNA NM_170707.3 +/. - c.1444C>T r.(?) p.(Arg482Trp)


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