Variant #0000690819 (NC_000010.10:g.89621905_89621906del, NM_000314.4:c.-2322_-2321del (PTEN))
| Chromosome |
10 |
| 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.89621905_89621906del |
| DNA change (hg38) |
- |
| Published as |
KLLN(NM_001126049.1):c.339_340del (p.(Ala115SerfsTer58)), KLLN(NM_001126049.1):c.339_340delAG (p.A115Sfs*58) |
| ISCN |
- |
| DB-ID |
KLLN_000006 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) |
0.00142 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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