Variant #0000281548 (NC_000009.11:g.139333054_139333057del, NC_000009.11(NM_019892.4):c.812+7_812+10del (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.139333054_139333057del |
DNA change (hg38) |
g.136438602_136438605del |
Published as |
INPP5E(NM_019892.5):c.812+7_812+10delAGGG, INPP5E(NM_019892.6):c.812+7_812+10delAGGG |
ISCN |
- |
DB-ID |
INPP5E_000032 |
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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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