Variant #0000609049 (NC_000004.11:g.120213532A>G, NM_019050.2:c.2388A>G (USP53))

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.120213532A>G
DNA change (hg38) g.119292377A>G
Published as USP53(NM_019050.2):c.2388A>G (p.S796=)
ISCN -
DB-ID C4orf3_000002
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) 0.0005 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-16 14:38:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4orf3 NM_001001701.3 -?/. - c.*6402T>C r.(=) p.(=)
USP53 NM_019050.2 -?/. - c.2388A>G r.(?) p.(Ser796=)


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