Variant #0000608189 (NC_000003.11:g.10128894_10128895del, NM_001018115.1:c.3412_3413del (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.10128894_10128895del
DNA change (hg38) g.10087210_10087211del
Published as FANCD2(NM_001319984.2):c.3412_3413delTT (p.L1138Dfs*34)
ISCN -
DB-ID FANCD2_000115
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.3412_3413del r.(?) p.(Leu1138AspfsTer34) -
FANCD2OS NM_173472.1 +/. - c.*44-5678_*44-5677del r.(=) p.(=) -


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