NEUROG2 neurogenin 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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36 |
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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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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | Atoh4 |
SYNONYM | Math4A |
SYNONYM | NGN2 |
SYNONYM | bHLHa8 |
SYNONYM | ngn-2 |
MIM | 606624 OMIM |
HGNC | HGNC:13805 HGNC |
Ensembl | ENSG00000178403 Ensembl |
AllianceGenome | HGNC:13805 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000313341.4 | hg38 | chr4 | 112,513,516 | 112,516,180 | 2,665 |
ENST00000313341.4 | hg19 | chr4 | 113,434,672 | 113,437,336 | 2,665 |
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