Variant #0000558675 (NC_000016.9:g.58052907G>A, NM_024598.3:c.641G>A (USB1))

Chromosome 16
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.58052907G>A
DNA change (hg38) g.58019003G>A
Published as USB1(NM_024598.3):c.641G>A (p.C214Y), USB1(NM_024598.4):c.641G>A (p.C214Y)
ISCN -
DB-ID ZNF319_000005 See all 2 reported entries
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) 0.00052 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF319 NM_020807.1 ?/. - c.-19768C>T r.(?) p.(=)
USB1 NM_024598.3 ?/. - c.641G>A r.(?) p.(Cys214Tyr)


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