ANO2 anoctamin 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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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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 | C12orf3 |
SYNONYM | TMEM16B |
MIM | 610109 OMIM |
HGNC | HGNC:1183 HGNC |
Ensembl | ENSG00000047617 Ensembl |
AllianceGenome | HGNC:1183 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000650848.1 | hg38 | chr12 | 5,562,654 | 5,945,228 | 382,575 |
ENST00000682330.1 | hg38 | chr12 | 5,562,655 | 5,945,259 | 382,605 |
ENST00000356134.9 | hg38 | chr12 | 5,562,654 | 5,946,232 | 383,579 |
ENST00000650848.1 | hg19 | chr12 | 5,671,820 | 6,054,394 | 382,575 |
ENST00000356134.9 | hg19 | chr12 | 5,671,820 | 6,055,398 | 383,579 |
ENST00000682330.1 | hg19 | chr12 | 5,671,821 | 6,054,425 | 382,605 |
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