Variant #0000619140 (NC_000023.10:g.151900113C>T, NM_001102576.1:c.-3227C>T (CSAG1))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.151900113C>T |
| DNA change (hg38) |
g.152736847= |
| Published as |
MAGEA12(NM_001166386.3):c.688G>A (p.A230T) |
| ISCN |
- |
| DB-ID |
MAGEA12_000017 |
| 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) |
6.0E-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 |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
|