Variant #0000269005 (NC_000003.11:g.10091084T>C, NM_001018115.1:c.1440T>C (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.10091084T>C
DNA change (hg38) g.10049400T>C
Published as FANCD2(NM_033084.3):c.1440T>C (p.H480=), FANCD2(NM_033084.6):c.1440T>C (p.H480=)
ISCN -
DB-ID FANCD2_000070 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.1440T>C r.(?) p.(His480=) -
FANCD2OS NM_173472.1 -?/. - c.*32175A>G r.(=) p.(=) -


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