Variant #0000250414 (NC_000002.11:g.58388642A>G, NC_000002.11(NM_018062.3):c.1020+15T>C (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.58388642A>G
DNA change (hg38) g.58161507A>G
Published as FANCL(NM_001114636.1):c.1035+15T>C
ISCN -
DB-ID FANCL_000012
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) 0.00011 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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.*1814A>G r.(=) p.(=) -
FANCL NM_018062.3 -?/. - c.1020+15T>C r.(=) p.(=) -


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