GRIN3B glutamate ionotropic receptor NMDA type subunit 3B
Information
- Symbol
- GRIN3B
- Type
- protein-coding
- Description
- glutamate ionotropic receptor NMDA type subunit 3B
- Entrez Gene ID
- 116444
- Genome
- hg19
- Position
- chr19:1,000,418-1,009,731
- Genome
- hg38
- Position
- chr19:1,000,419-1,009,732
- MIM
- 606651 OMIM
- HGNC
- HGNC:16768 HGNC
- Ensembl
- ENSG00000116032 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 14 |
Likely benign | 0 | 8 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 212 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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234 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | GluN3B |
SYNONYM | NR3B |
MIM | 606651 OMIM |
HGNC | HGNC:16768 HGNC |
Ensembl | ENSG00000116032 Ensembl |
AllianceGenome | HGNC:16768 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000234389.3 | hg38 | chr19 | 1,000,419 | 1,009,732 | 9,314 |
ENST00000234389.3 | hg19 | chr19 | 1,000,418 | 1,009,731 | 9,314 |
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