Variant #0001065860 (NC_000012.11:g.122353791G>A, NM_144668.5:c.-2831G>A (WDR66))

Chromosome 12
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.122353791G>A
DNA change (hg38) -
Published as PSMD9(NM_002813.7):c.585G>A (p.(Arg195=))
ISCN -
DB-ID PSMD9_000002
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) 0.00038 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +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     
PSMD9 NM_002813.5 ?/. - c.585G>A r.(?) p.(=)
WDR66 NM_144668.5 ?/. - c.-2831G>A r.(?) p.(=)


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