Variant #0000523560 (NC_000004.11:g.9270413T>G, NM_001256862.1:c.*4223T>G (USP17L21))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.9270413T>G
DNA change (hg38) g.9268687T>G
Published as USP17L22(NM_001256863.1):c.1069T>G (p.S357A)
ISCN -
DB-ID USP17L21_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP17L21 NM_001256862.1 -/. - c.*4223T>G r.(=) p.(=)
USP17L22 NM_001256863.1 -/. - c.1069T>G r.(?) p.(Ser357Ala)


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