Variant #0000521518 (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) |
g.122934580_122934582del |
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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|