Variant #0000332085 (NC_000008.10:g.30700808_30700811del, NM_031271.3:c.5725_5728del (TEX15))
| Chromosome |
8 |
| 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.30700808_30700811del |
| DNA change (hg38) |
g.30843292_30843295del |
| Published as |
TEX15(NM_001350162.2):c.6874_6877delTCAC (p.S2292Kfs*11), TEX15(NM_031271.3):c.5725_5728del (p.?) |
| ISCN |
- |
| DB-ID |
TEX15_000002 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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