Variant #0000532200 (NC_000007.13:g.4841545G>A, NM_020144.4:c.*57983C>T (PAPOLB))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.4841545G>A
DNA change (hg38) g.4801914G>A
Published as RADIL(NM_018059.5):c.2581C>T (p.R861W)
ISCN -
DB-ID PAPOLB_000003
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) 0.00049 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RADIL NM_018059.4 ?/. - c.2581C>T r.(?) p.(Arg861Trp)
PAPOLB NM_020144.4 ?/. - c.*57983C>T r.(=) p.(=)


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