Variant #0000306729 (NC_000007.13:g.4839879C>G, NM_020144.4:c.*59649G>C (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.4839879C>G
DNA change (hg38) g.4800248C>G
Published as RADIL(NM_018059.4):c.2905G>C (p.E969Q)
ISCN -
DB-ID RADIL_000001
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RADIL NM_018059.4 ?/. - c.2905G>C r.(?) p.(Glu969Gln)
PAPOLB NM_020144.4 ?/. - c.*59649G>C r.(=) p.(=)


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