Variant #0000516498 (NC_000002.11:g.58390230del, NC_000002.11(NM_018062.3):c.776-10del (FANCL))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58390230del
DNA change (hg38) g.58163095del
Published as FANCL(NM_001114636.1):c.791-10delT
ISCN -
DB-ID FANCL_000022
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*3402del r.(?) p.(=) -
FANCL NM_018062.3 -?/. - c.776-10del r.(=) p.(=) -


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