Variant #0000519907 (NC_000003.11:g.46037206G>T, NC_000003.11(NM_024513.3):c.-113+8C>A (FYCO1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46037206G>T
DNA change (hg38) g.45995714G>T
Published as FYCO1(NM_024513.3):c.-113+8C>A
ISCN -
DB-ID CXCR6_000018
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_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 2020-03-23 16:13:27 +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.*48204G>T r.(=) p.(=)
FYCO1 NM_024513.3 -?/. - c.-113+8C>A r.(=) p.(=)


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