Variant #0000975839 (NC_000003.11:g.45972345G>A, NC_000003.11(NM_024513.3):c.4251+218C>T (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.45972345G>A
DNA change (hg38) -
Published as FYCO1(NM_001386424.1):c.4364C>T (p.(Ser1455Phe))
ISCN -
DB-ID CXCR6_000038
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR6 NM_006564.1 ?/. - c.-12709G>A r.(?) p.(=)
FYCO1 NM_024513.3 ?/. - c.4251+218C>T r.(=) p.(=)


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