Variant #0000911791 (NC_000003.11:g.10078042G>A, NC_000003.11(NM_001018115.1):c.491+19G>A (FANCD2))

Chromosome 3
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.10078042G>A
DNA change (hg38) -
Published as FANCD2(NM_033084.3):c.491+19G>A
ISCN -
DB-ID FANCD2_000131
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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCD2 NM_001018115.1 -?/. - c.491+19G>A r.(=) p.(=) -
FANCD2OS NM_173472.1 -?/. - c.*45217C>T r.(=) p.(=) -


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