Variant #0000288763 (NC_000023.10:g.122319733T>C, NM_007325.4:c.159T>C (GRIA3))
| 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.122319733T>C |
| DNA change (hg38) |
g.123185881T>C |
| Published as |
GRIA3(NM_000828.4):c.159T>C (p.F53=), GRIA3(NM_001256743.2):c.158T>C (p.F53S), GRIA3(NM_007325.5):c.158T>C (p.F53S) |
| ISCN |
- |
| DB-ID |
GRIA3_000038 See all 3 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) |
0.00088 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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