Variant #0000799298 (NC_000001.10:g.27695863T>C, NM_003665.2:c.764A>G (FCN3))

Chromosome 1
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.27695863T>C
DNA change (hg38) -
Published as FCN3(NM_003665.2):c.764A>G (p.Y255C), FCN3(NM_003665.4):c.764A>G (p.Y255C)
ISCN -
DB-ID FCN3_000005 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 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FCN3 NM_003665.2 ?/. - c.764A>G r.(?) p.(Tyr255Cys)
MAP3K6 NM_004672.3 ?/. - c.-2775A>G r.(?) p.(=)


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