Variant #0000679522 (NC_000012.11:g.42866205C>T, NM_153026.2:c.114G>A (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.42866205C>T
DNA change (hg38) -
Published as PRICKLE1(NM_153026.2):c.114G>A (p.P38=), PRICKLE1(NM_153026.3):c.114G>A (p.P38=)
ISCN -
DB-ID PRICKLE1_000033 See all 2 reported entries
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) 0.0025 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRICKLE1 NM_001144881.1 -?/. - c.114G>A r.(?) p.(Pro38=)
PRICKLE1 NM_153026.2 -?/. - c.114G>A r.(?) p.(Pro38=)


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