Variant #0000724027 (NC_000012.11:g.42858478G>A, NM_153026.2:c.1358C>T (PRICKLE1))

Chromosome 12
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.42858478G>A
DNA change (hg38) -
Published as PRICKLE1(NM_153026.2):c.1358C>T (p.T453I)
ISCN -
DB-ID PRICKLE1_000041
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRICKLE1 NM_001144881.1 -?/. - c.1358C>T r.(?) p.(Thr453Ile)
PRICKLE1 NM_153026.2 -?/. - c.1358C>T r.(?) p.(Thr453Ile)


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