Variant #0000692401 (NC_000017.10:g.5064836G>A, NM_004505.2:c.2842G>A (USP6))

Chromosome 17
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.5064836G>A
DNA change (hg38) -
Published as USP6(NM_001304284.1):c.2842G>A (p.G948S)
ISCN -
DB-ID USP6_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP6 NM_004505.2 ?/. - c.2842G>A r.(?) p.(Gly948Ser)
ZNF232 NM_014519.2 ?/. - c.-39094C>T r.(?) p.(=)


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