Variant #0000532692 (NC_000007.13:g.77789464G>C, NM_012301.3:c.2723C>G (MAGI2))
| Chromosome |
7 |
| 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.77789464G>C |
| DNA change (hg38) |
g.78160147G>C |
| Published as |
MAGI2(NM_012301.3):c.2723C>G (p.(Pro908Arg)), MAGI2(NM_012301.4):c.2723C>G (p.P908R) |
| ISCN |
- |
| DB-ID |
MAGI2_000051 See all 2 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) |
0.00031 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|