Variant #0000999993 (NC_000012.11:g.42853796C>T, NM_153026.2:c.2311G>A (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.42853796C>T
DNA change (hg38) -
Published as PRICKLE1(NM_153026.2):c.2311G>A (p.(Asp771Asn))
ISCN -
DB-ID PRICKLE1_000007 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) 1.0E-5 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 2024-08-28 13:16:32 +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.2311G>A r.(?) p.(Asp771Asn)
PRICKLE1 NM_153026.2 ?/. - c.2311G>A r.(?) p.(Asp771Asn)


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