Variant #0001093079 (NC_000012.11:g.80889670A>G, NC_000012.11(NM_001145026.2):c.1883-108A>G (PTPRQ))

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.80889670A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr12_009478
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2541561769
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-10-13 11:07:03 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPRQ NM_001145026.2 ?/. - c.1883-108A>G r.(?) p.(?)


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