Variant #0000803983 (NC_000009.11:g.139327607_139327608insCCTCTAGCCACGCCCACC, NC_000009.11(NM_019892.4):c.1159+7_1159+8insTGGCTAGAGGGGTGGGCG (INPP5E))
| Chromosome |
9 |
| 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.139327607_139327608insCCTCTAGCCACGCCCACC |
| DNA change (hg38) |
- |
| Published as |
INPP5E(NM_001318502.2):c.1159+7_1159+8insTGGCTAGAGGGGTGGGCG, INPP5E(NM_019892.5):c.1159+7_1159+8insTGGCTAGAGGGGTGGGCG, INPP5E(NM_019892.6):c.1159+7... |
| ISCN |
- |
| DB-ID |
INPP5E_000052 See all 3 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) |
Retrieve |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
|