Variant #0000523551 (NC_000004.11:g.9250440T>G, NM_001256859.1:c.85T>G (USP17L18))

Chromosome 4
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.9250440T>G
DNA change (hg38) g.9248714T>G
Published as USP17L18(NM_001256859.1):c.85T>G (p.(Phe29Val))
ISCN -
DB-ID USP17L17_000006
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
USP17L17 NM_001256857.1 -?/. - c.*3243T>G r.(=) p.(=)
USP17L18 NM_001256859.1 -?/. - c.85T>G r.(?) p.(Phe29Val)
USP17L19 NM_001256860.1 -?/. - c.-4664T>G r.(?) p.(=)


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