Variant #0000863088 (NC_000012.11:g.58131545C>T, NC_000012.11(NM_014770.3):c.161-2335G>A (AGAP2))
| Chromosome |
12 |
| 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.58131545C>T |
| DNA change (hg38) |
- |
| Published as |
AGAP2(NM_001122772.2):c.485G>A (p.G162D, p.(Gly162Asp)) |
| ISCN |
- |
| DB-ID |
AGAP2_000002 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) |
0.00014 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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