Variant #0001075647 (NC_000012.11:g.81004240T>C, NM_001145026.2:c.4754T>C (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.81004240T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID PTPRQ_000136
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1898506897
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 2026-04-28 12:12:09 +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.4754T>C r.(?) p.(Ile1585Thr)


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