Variant #0001034318 (NC_000004.11:g.123855735_123855737del, NM_145207.2:c.989_991del (SPATA5))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.123855735_123855737del |
| DNA change (hg38) |
- |
| Published as |
SPATA5(NM_145207.2):c.989_991delCAA (p.T330del), SPATA5(NM_145207.3):c.989_991del (p.(Thr330del)), SPATA5(NM_145207.3):c.989_991delCAA (p.T330del) |
| ISCN |
- |
| DB-ID |
SPATA5_000015 See all 11 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 |
2025-05-05 21:14:00 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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