Variant #0000288763 (NC_000023.10:g.122319733T>C, GRIA3(NM_007325.4):c.159T>C)
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_001256743.1):c.158T>C (p.F53S), GRIA3(NM_001256743.2):c.158T>C (p.F53S) |
ISCN |
- |
DB-ID |
GRIA3_000038 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) |
0.00088 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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