Variant #0000912604 (NC_000006.11:g.99883683A>G, NM_001080481.1:c.2354T>C (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.99883683A>G
DNA change (hg38) -
Published as USP45(NM_001080481.3):c.2354T>C (p.V785A)
ISCN -
DB-ID PNISR_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.2354T>C r.(?) p.(Val785Ala)
PNISR NM_032870.2 ?/. - c.-10704T>C r.(?) p.(=)


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