Variant #0000293766 (NC_000019.9:g.18280044C>T, NM_005027.3:c.2127C>T (PIK3R2))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.18280044C>T |
| DNA change (hg38) |
g.18169234C>T |
| Published as |
PIK3R2(NM_005027.2):c.2127C>T (p.(Thr709=)), PIK3R2(NM_005027.3):c.2127C>T (p.T709=), PIK3R2(NM_005027.4):c.2127C>T (p.T709=) |
| ISCN |
- |
| DB-ID |
PIK3R2_000022 See all 4 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.04937 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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