Variant #0000288013 (NC_000003.11:g.45965190G>A, NM_024513.3:c.4319C>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.45965190G>A
DNA change (hg38) g.45923698G>A
Published as FYCO1(NM_024513.3):c.4319C>T (p.T1440I)
ISCN -
DB-ID FYCO1_000003
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) 0.00352 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 2020-03-23 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.-19864G>A r.(?) p.(=)
FYCO1 NM_024513.3 -?/. - c.4319C>T r.(?) p.(Thr1440Ile)


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