Variant #0000926681 (NC_000017.10:g.80403807C>T, NM_001033046.3:c.231G>A (C17orf62))

Chromosome 17
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.80403807C>T
DNA change (hg38) -
Published as CYBC1(NM_001033046.4):c.231G>A (p.K77=)
ISCN -
DB-ID C17orf62_000016
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf62 NM_001033046.3 -?/. - c.231G>A r.(?) p.(Lys77=)
HEXDC NM_173620.2 -?/. - c.*3339C>T r.(=) p.(=)
OGFOD3 NM_175902.4 -?/. - c.-27446G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.