Variant #0000523554 (NC_000004.11:g.9251597C>A, NM_001256859.1:c.1242C>A (USP17L18))

Chromosome 4
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.9251597C>A
DNA change (hg38) g.9249871C>A
Published as USP17L18(NM_001256859.1):c.1242C>A (p.C414*)
ISCN -
DB-ID USP17L17_000009
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 2020-06-16 12:37:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP17L17 NM_001256857.1 ?/. - c.*4400C>A r.(=) p.(=)
USP17L18 NM_001256859.1 ?/. - c.1242C>A r.(?) p.(Cys414Ter)
USP17L19 NM_001256860.1 ?/. - c.-3507C>A r.(?) p.(=)


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