Variant #0000288008 (NC_000003.11:g.46008983G>A, NM_024513.3:c.1843C>T (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.46008983G>A
DNA change (hg38) g.45967491G>A
Published as FYCO1(NM_024513.3):c.1843C>T (p.R615W, p.(Arg615Trp))
ISCN -
DB-ID FYCO1_000009 See all 2 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) 0.01072 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 2018-01-15 20:58:59 +01:00 (CET)
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.*19981G>A r.(=) p.(=)
FYCO1 NM_024513.3 -?/. - c.1843C>T r.(?) p.(Arg615Trp)


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