Variant #0000573335 (NC_000023.10:g.122336603dup, NC_000023.10(NM_007325.4):c.268+16761dup (GRIA3))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.122336603dup |
| DNA change (hg38) |
g.123202751dup |
| Published as |
GRIA3(NM_000828.4):c.268+16761dupG, GRIA3(NM_001256743.1):c.380dupG, GRIA3(NM_001256743.2):c.380dupG (p.G128Wfs*16), GRIA3(NM_001256743.2):c.384del... |
| ISCN |
- |
| DB-ID |
GRIA3_000022 See all 5 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) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
|