Variant #0000997342 (NC_000008.10:g.7834645C>T, NM_001256872.1:c.-3870G>A (USP17L8))

Chromosome 8
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.7834645C>T
DNA change (hg38) -
Published as USP17L2(NM_001256871.1):c.863G>A (p.(Gly288Asp))
ISCN -
DB-ID USP17L8_000012
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP17L3 NM_001256871.1 -?/. - c.863G>A r.(?) p.(Gly288Asp)
USP17L8 NM_001256872.1 -?/. - c.-3870G>A r.(?) p.(=)
FAM66E NR_027424.1 -?/. - n.611-8049C>T r.(?) -


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