Variant #0000327017 (NC_000002.11:g.58311254C>A, NM_018062.3:c.*75646G>T (FANCL))

Chromosome 2
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.58311254C>A
DNA change (hg38) g.58084119C>A
Published as VRK2(NM_001130480.2):c.167C>A (p.(Ala56Glu))
ISCN -
DB-ID VRK2_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) 2.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
VRK2 NM_006296.5 ?/. - c.167C>A r.(?) p.(Ala56Glu) -
FANCL NM_018062.3 ?/. - c.*75646G>T r.(=) p.(=) -


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