Variant #0000679515 (NC_000012.11:g.42853871G>A, NM_153026.2:c.2236C>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.42853871G>A
DNA change (hg38) -
Published as PRICKLE1(NM_001144881.1):c.2236C>T (p.(Pro746Ser)), PRICKLE1(NM_153026.3):c.2236C>T (p.P746S)
ISCN -
DB-ID PRICKLE1_000022 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) 0.01071 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.2236C>T r.(?) p.(Pro746Ser)
PRICKLE1 NM_153026.2 -?/. - c.2236C>T r.(?) p.(Pro746Ser)


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