Variant #0000348195 (NC_000003.11:g.45965188G>T, NM_024513.3:c.4321C>A (FYCO1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45965188G>T
DNA change (hg38) g.45923696G>T
Published as FYCO1(NM_024513.3):c.4321C>A (p.P1441T)
ISCN -
DB-ID FYCO1_000021 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) 0.00057 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.-19866G>T r.(?) p.(=)
FYCO1 NM_024513.3 ?/. - c.4321C>A r.(?) p.(Pro1441Thr)


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