Variant #0001051294 (NC_000003.11:g.46008475_46008477dup, NM_024513.3:c.2351_2353dup (FYCO1))

Chromosome 3
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.46008475_46008477dup
DNA change (hg38) -
Published as FYCO1(NM_024513.4):c.2351_2353dup (p.(Glu784dup))
ISCN -
DB-ID CXCR6_000044
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR6 NM_006564.1 ?/. - c.*19473_*19475dup r.(=) p.(=)
FYCO1 NM_024513.3 ?/. - c.2351_2353dup r.(?) p.(Glu784dup)


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