Variant #0000711844 (NC_000012.11:g.80839436A>G, NM_001145026.2:c.329A>G (PTPRQ))

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.80839436A>G
DNA change (hg38) g.80445656A>G
Published as -
ISCN -
DB-ID PTPRQ_000087
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs756626854
Origin CLASSIFICATION record
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 2021-01-14 16:35:02 +01:00 (CET)
Date last edited 2023-11-08 15:48:34 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPRQ NM_001145026.2 -?/. - c.329A>G r.(?) p.(Lys110Arg)


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