Variant #0000978686 (NC_000009.11:g.35077022_35077023dup, NM_004629.1:c.723_724dup (FANCG))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35077022_35077023dup
DNA change (hg38) -
Published as FANCG(NM_004629.2):c.723_724dup (p.(Arg242HisfsTer33))
ISCN -
DB-ID FANCG_000083
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCG NM_004629.1 ?/. - c.723_724dup r.(?) p.(Arg242Hisfs*33) -
VCP NM_007126.3 ?/. - c.-4672_-4671dup r.(?) p.(=) -


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