Variant #0000038002 (NC_000012.11:g.13828688C>T, NM_000834.3:c.1116G>A (GRIN2B))
Chromosome |
12 |
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.13828688C>T |
DNA change (hg38) |
g.13675754C>T |
Published as |
1116A>G |
ISCN |
- |
DB-ID |
GRIN2B_000021 |
Variant remarks |
variant reported erroneously or reference sequence is rare allele |
Reference |
PubMed: Endele 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
? |
Frequency |
1/630 cases |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2014-07-01 23:23:20 +02:00 (CEST) |
Date last edited |
2014-07-01 23:23:45 +02:00 (CEST) |

Variant on transcripts
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