Variant #0000521514 (NC_000004.11:g.123848876G>A, NM_145207.2:c.251G>A (SPATA5))
Chromosome |
4 |
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.123848876G>A |
DNA change (hg38) |
g.122927721G>A |
Published as |
SPATA5(NM_001317799.1):c.248G>A (p.(Arg83Gln)), SPATA5(NM_145207.2):c.251G>A (p.R84Q) |
ISCN |
- |
DB-ID |
SPATA5_000006 See all 5 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) |
7.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
|