Variant #0000548100 (NC_000012.11:g.42854140G>A, NM_153026.2:c.1967C>T (PRICKLE1))

Chromosome 12
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.42854140G>A
DNA change (hg38) g.42460338G>A
Published as PRICKLE1(NM_153026.2):c.1967C>T (p.T656I)
ISCN -
DB-ID PRICKLE1_000027
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRICKLE1 NM_001144881.1 ?/. - c.1967C>T r.(?) p.(Thr656Ile)
PRICKLE1 NM_153026.2 ?/. - c.1967C>T r.(?) p.(Thr656Ile)


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