NEUROG3 neurogenin 3
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 12 |
| Likely pathogenic | 0 | 8 |
| Benign | 0 | 16 |
| Likely benign | 0 | 68 |
| Conflicting classifications of pathogenicity | 0 | 6 |
| Uncertain significance | 0 | 146 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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18 |
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226 |
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2 |
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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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 |
Prediction | |||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | Atoh5 |
| SYNONYM | Math4B |
| SYNONYM | NGN-3 |
| SYNONYM | bHLHa7 |
| SYNONYM | ngn3 |
| MIM | 604882 OMIM |
| HGNC | HGNC:13806 HGNC |
| Ensembl | ENSG00000122859 Ensembl |
| AllianceGenome | HGNC:13806 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000242462.5 | hg38 | chr10 | 69,571,698 | 69,573,422 | 1,725 |
| ENST00000242462.5 | hg19 | chr10 | 71,331,454 | 71,333,178 | 1,725 |
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