Variant #0000558669 (NC_000016.9:g.58031932C>T, NM_024598.3:c.-3456C>T (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.58031932C>T
DNA change (hg38) g.57998028C>T
Published as ZNF319(NM_020807.2):c.238G>A (p.V80M)
ISCN -
DB-ID ZNF319_000001
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) 5.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF319 NM_020807.1 ?/. - c.238G>A r.(?) p.(Val80Met)
USB1 NM_024598.3 ?/. - c.-3456C>T r.(?) p.(=)


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