Variant #0000719446 (NC_000003.11:g.46010032_46010050del, NM_024513.3:c.778_796del (FYCO1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46010032_46010050del
DNA change (hg38) -
Published as FYCO1(NM_024513.4):c.778_796delAACCAGGAGCTGAGGGCAG (p.N260Lfs*30)
ISCN -
DB-ID CXCR6_000015
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR6 NM_006564.1 +/. - c.*21030_*21048del r.(=) p.(=)
FYCO1 NM_024513.3 +/. - c.778_796del r.(?) p.(Asn260LeufsTer30)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.