Variant #0000325786 (NC_000017.10:g.80400236C>A, NM_001033046.3:c.*1644G>T (C17orf62))

Chromosome 17
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.80400236C>A
DNA change (hg38) g.82442360C>A
Published as HEXDC(NM_173620.2):c.1526C>A (p.(Ala509Glu))
ISCN -
DB-ID C17orf62_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) 0.00126 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf62 NM_001033046.3 ?/. - c.*1644G>T r.(=) p.(=)
HEXDC NM_173620.2 ?/. - c.1526C>A r.(?) p.(Ala509Glu)
OGFOD3 NM_175902.4 ?/. - c.-23875G>T r.(?) p.(=)


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