Variant #0000308038 (NC_000005.9:g.171765715_171765717del, NM_001017995.2:c.2395_2397del (SH3PXD2B))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171765715_171765717del |
| DNA change (hg38) |
g.172338711_172338713del |
| Published as |
SH3PXD2B(NM_001017995.2):c.2395_2397del (p.(Leu799del)), SH3PXD2B(NM_001017995.2):c.2395_2397delCTC (p.L799del) |
| ISCN |
- |
| DB-ID |
SH3PXD2B_000003 See all 2 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2021-02-08 18:36:18 +01:00 (CET) |

Variant on transcripts
|