Variant #0000281137 (NC_000023.10:g.122336603dup, GRIA3(NM_007325.4):c.268+16761dup)
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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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