Variant #0000924048 (NC_000004.11:g.120213810G>A, NM_019050.2:c.2666G>A (USP53))

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.120213810G>A
DNA change (hg38) -
Published as USP53(NM_019050.2):c.2666G>A (p.C889Y)
ISCN -
DB-ID C4orf3_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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4orf3 NM_001001701.3 ?/. - c.*6124C>T r.(=) p.(=)
USP53 NM_019050.2 ?/. - c.2666G>A r.(?) p.(Cys889Tyr)


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