Variant #0000503753 (NC_000001.10:g.156108325G>A, NM_170707.3:c.1745G>A (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.156108325G>A
DNA change (hg38) g.156138534G>A
Published as LMNA(NM_001257374.1):c.1409G>A (p.(Arg470His)), LMNA(NM_170707.2):c.1745G>A (p.R582H), LMNA(NM_170707.4):c.1745G>A (p.R582H)
ISCN -
DB-ID LMNA_000016 See all 6 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMNA NM_170707.3 +/. - c.1745G>A r.(?) p.(Arg582His)


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