Variant #0000519895 (NC_000003.11:g.46008841G>A, NM_024513.3:c.1985C>T (FYCO1))

Chromosome 3
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.46008841G>A
DNA change (hg38) g.45967349G>A
Published as FYCO1(NM_024513.3):c.1985C>T (p.S662F, p.(Ser662Phe))
ISCN -
DB-ID CXCR6_000008 See all 3 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) 0.00164 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR6 NM_006564.1 -/. - c.*19839G>A r.(=) p.(=)
FYCO1 NM_024513.3 -/. - c.1985C>T r.(?) p.(Ser662Phe)


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