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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