Variant #0000976107 (NC_000004.11:g.123844298A>C, NM_145207.2:c.1A>C (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.123844298A>C |
DNA change (hg38) |
- |
Published as |
SPATA5(NM_145207.2):c.1A>C (p.M1?), SPATA5(NM_145207.3):c.1A>C (p.(Met1?), p.M1?) |
ISCN |
- |
DB-ID |
SPATA5_000021 See all 7 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) |
9.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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