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 International |
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) |

Variant on transcripts
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