Variant #0000510320 (NC_000002.11:g.178682558_178682559insTATAAAC, NC_000002.11(NM_016953.3):c.1644+26_1644+27insGTTTATA (PDE11A))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.178682558_178682559insTATAAAC
DNA change (hg38) g.177817831_177817832insTATAAAC
Published as PDE11A(NM_016953.4):c.1644+28_1644+29insTTATAGT
ISCN -
DB-ID PDE11A_000015
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) 0.31441 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE11A NM_016953.3 -/. - c.1644+26_1644+27insGTTTATA r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.