Variant #0000691334 (NC_000012.11:g.42853845G>C, NM_153026.2:c.2262C>G (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.42853845G>C
DNA change (hg38) -
Published as PRICKLE1(NM_153026.2):c.2262C>G (p.L754=)
ISCN -
DB-ID PRICKLE1_000040
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) 2.0E-5 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 2020-09-15 15:50:26 +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     
PRICKLE1 NM_001144881.1 -?/. - c.2262C>G r.(?) p.(Leu754=)
PRICKLE1 NM_153026.2 -?/. - c.2262C>G r.(?) p.(Leu754=)


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