Variant #0000801238 (NC_000003.11:g.46003862C>T, NM_024513.3:c.3292G>A (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.46003862C>T
DNA change (hg38) -
Published as FYCO1(NM_024513.3):c.3292G>A (p.A1098T)
ISCN -
DB-ID CXCR6_000028
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) 3.0E-5 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 2021-09-17 14:40:49 +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     
CXCR6 NM_006564.1 ?/. - c.*14860C>T r.(=) p.(=)
FYCO1 NM_024513.3 ?/. - c.3292G>A r.(?) p.(Ala1098Thr)


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