Variant #0000923988 (NC_000003.11:g.64132648_64132653del, NM_198859.3:c.1526_1531del (PRICKLE2))

Chromosome 3
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.64132648_64132653del
DNA change (hg38) -
Published as PRICKLE2(NM_198859.4):c.1526_1531delAGGAAG (p.E509_E510del)
ISCN -
DB-ID PRICKLE2_000034
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 2023-04-16 21:50:28 +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     
PRICKLE2 NM_198859.3 ?/. - c.1526_1531del r.(?) p.(Glu509_Glu510del)


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