Variant #0000676771 (NC_000003.11:g.10115043C>T, NM_001018115.1:c.2712C>T (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.10115043C>T
DNA change (hg38) -
Published as FANCD2(NM_001018115.1):c.2712C>T (p.(Asn904=)), FANCD2(NM_033084.6):c.2712C>T (p.N904=)
ISCN -
DB-ID FANCD2_000086 See all 2 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) 0.00709 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCD2 NM_001018115.1 -?/. - c.2712C>T r.(?) p.(Asn904=) -
FANCD2OS NM_173472.1 -?/. - c.*8216G>A r.(=) p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.