Variant #0001056147 (NC_000017.10:g.65337736_65337738dup, NC_000017.10(NM_002816.3):c.1161+567_1162-565dup (PSMD12))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65337736_65337738dup
DNA change (hg38) -
Published as PSMD12(NM_002816.5):c.1161+567_1162-565dup
ISCN -
DB-ID PSMD12_000022
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 2025-11-01 13:22:20 +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     
PSMD12 NM_002816.3 -?/. - c.1161+567_1162-565dup r.(?) p.(=)


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