Variant #0000510319 (NC_000002.11:g.178494177_178494179dup, NM_016953.3:c.2761_2763dup (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.178494177_178494179dup
DNA change (hg38) g.177629449_177629451dup
Published as PDE11A(NM_016953.4):c.2761_2763dupTCC (p.S921dup)
ISCN -
DB-ID PDE11A_000014
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE11A NM_016953.3 -/. - c.2761_2763dup r.(?) p.(Ser921dup)


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