Variant #0000288010 (NC_000003.11:g.46008789C>T, NM_024513.3:c.2037G>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.46008789C>T
DNA change (hg38) g.45967297C>T
Published as FYCO1(NM_024513.3):c.2037G>A (p.A679=)
ISCN -
DB-ID FYCO1_000007
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) 0.00038 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 2020-06-12 18:46:57 +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.*19787C>T r.(=) p.(=)
FYCO1 NM_024513.3 -?/. - c.2037G>A r.(?) p.(Ala679=)


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