Variant #0000944302 (NC_000012.11:g.80472134del, NM_001145026.2:c.1069del (PTPRQ))
Individual ID |
00441463 |
Chromosome |
12 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.80472134del |
DNA change (hg38) |
g.80865913del |
Published as |
1057_1057delC |
ISCN |
- |
DB-ID |
PTPRQ_000113 |
Variant remarks |
- |
Reference |
PubMed: Yang 2021 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2023-11-07 19:48:55 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
Screenings
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