Variant #0000574073 (NC_000023.10:g.14863136A>G, NM_001018113.1:c.1769T>C (FANCB))

Chromosome X
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.14863136A>G
DNA change (hg38) g.14845014A>G
Published as FANCB(NM_001018113.1):c.1769T>C (p.F590S), FANCB(NM_001018113.3):c.1769T>C (p.F590S)
ISCN -
DB-ID FANCB_000048 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) 0.00161 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCB NM_001018113.1 -?/. - c.1769T>C r.(?) p.(Phe590Ser) -


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