Variant #0000977404 (NC_000006.11:g.99958092del, NM_001080481.1:c.7del (USP45))

Chromosome 6
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.99958092del
DNA change (hg38) -
Published as USP45(NM_001080481.1):c.7delG (p.V3*), USP45(NM_001080481.3):c.7delG (p.V3*), USP45(NM_001346021.3):c.7delG (p.V3*), USP45(NM_001346022.3):c.7del ...
ISCN -
DB-ID USP45_000008 See all 4 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
USP45 NM_001080481.1 ?/. - c.7del r.(?) p.(Val3*)


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