Variant #0001032557 (NC_000002.11:g.178969171_178969172del, NM_016953.3:c.-32007_-32006del (PDE11A))

Chromosome 2
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.178969171_178969172del
DNA change (hg38) -
Published as PDE11A(NM_001077197.2):c.20_21del (p.(Arg7ThrfsTer30))
ISCN -
DB-ID PDE11A_000033
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 2025-05-05 21:14:00 +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     
PDE11A NM_016953.3 ?/. - c.-32007_-32006del r.(?) p.(=)


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