SBNO2 strawberry notch homolog 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 20 |
Uncertain significance | 0 | 226 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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248 |
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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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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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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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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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 |
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SYNONYM | KIAA0963 |
SYNONYM | SNO |
SYNONYM | STNO |
MIM | 615729 OMIM |
HGNC | HGNC:29158 HGNC |
Ensembl | ENSG00000064932 Ensembl |
AllianceGenome | HGNC:29158 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000438103.6 | hg38 | chr19 | 1,107,637 | 1,132,221 | 24,585 |
ENST00000587024.5 | hg38 | chr19 | 1,107,641 | 1,174,256 | 66,616 |
ENST00000361757.8 | hg38 | chr19 | 1,107,638 | 1,174,268 | 66,631 |
ENST00000438103.6 | hg19 | chr19 | 1,107,636 | 1,132,220 | 24,585 |
ENST00000361757.8 | hg19 | chr19 | 1,107,637 | 1,174,267 | 66,631 |
ENST00000587024.5 | hg19 | chr19 | 1,107,640 | 1,174,255 | 66,616 |
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