Variant #0000558671 (NC_000016.9:g.58036516C>T, NM_024598.3:c.232C>T (USB1))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.58036516C>T
DNA change (hg38) g.58002612C>T
Published as USB1(NM_001204911.2):c.232C>T (p.R78*)
ISCN -
DB-ID USB1_000008 See all 3 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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF319 NM_020807.1 +/. - c.-3377G>A r.(?) p.(=)
USB1 NM_024598.3 +/. - c.232C>T r.(?) p.(Arg78Ter)


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