Variant #0000703986 (NC_000012.11:g.80943396A>G, NM_001145026.2:c.4168A>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.80943396A>G
DNA change (hg38) g.80549617A>G
Published as -
ISCN -
DB-ID PTPRQ_000086
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs757316770
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2020-11-16 15:41:01 +01:00 (CET)
Date last edited 2023-11-08 16:26:40 +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.4168A>G r.(?) p.(Met1390Val)


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