Variant #0000517335 (NC_000003.11:g.10133890G>A, NM_001018115.1:c.3803G>A (FANCD2))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.10133890G>A
DNA change (hg38) g.10092206G>A
Published as FANCD2(NM_001018115.1):c.3803G>A (p.(Trp1268*))
ISCN -
DB-ID FANCD2_000025 See all 4 reported entries
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCD2 NM_001018115.1 +/. - c.3803G>A r.(?) p.(Trp1268Ter) -
FANCD2OS NM_173472.1 +/. - c.*44-10675C>T r.(=) p.(=) -


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