Variant #0000280946 (NC_000003.11:g.46010077C>T, NM_024513.3:c.749G>A (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.46010077C>T
DNA change (hg38) g.45968585C>T
Published as FYCO1(NM_024513.4):c.749G>A (p.R250Q)
ISCN -
DB-ID FYCO1_000016 See all 6 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) 0.84629 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CXCR6 NM_006564.1 -/. - c.*21075C>T r.(=) p.(=)
FYCO1 NM_024513.3 -/. - c.749G>A r.(?) p.(Arg250Gln)


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