Variant #0000970822 (NC_000023.10:g.14875966_14875968del, NC_000023.10(NM_001018113.1):c.1197+19_1197+21del (FANCB))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.14875966_14875968del
DNA change (hg38) -
Published as FANCB(NM_001018113.1):c.1197+19_1197+21delCTT, FANCB(NM_001018113.3):c.1197+19_1197+21delCTT
ISCN -
DB-ID FANCB_000072 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCB NM_001018113.1 -/. - c.1197+19_1197+21del r.(=) p.(=) -


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