NRGN neurogranin
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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
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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 |
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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 |
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SYNONYM | RC3 |
SYNONYM | hng |
MIM | 602350 OMIM |
HGNC | HGNC:8000 HGNC |
Ensembl | ENSG00000154146 Ensembl |
AllianceGenome | HGNC:8000 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000284292.11 | hg38 | chr11 | 124,739,942 | 124,747,210 | 7,269 |
ENST00000412681.2 | hg38 | chr11 | 124,740,045 | 124,747,206 | 7,162 |
ENST00000284292.11 | hg19 | chr11 | 124,609,838 | 124,617,106 | 7,269 |
ENST00000412681.2 | hg19 | chr11 | 124,609,941 | 124,617,102 | 7,162 |
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