ASIC1 acid sensing ion channel subunit 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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
Search Word
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | ACCN2 |
SYNONYM | ASIC |
SYNONYM | BNaC2 |
MIM | 602866 OMIM |
HGNC | HGNC:100 HGNC |
Ensembl | ENSG00000110881 Ensembl |
AllianceGenome | HGNC:100 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000552438.5 | hg38 | chr12 | 50,073,575 | 50,083,277 | 9,703 |
ENST00000228468.8 | hg38 | chr12 | 50,057,548 | 50,083,611 | 26,064 |
ENST00000447966.7 | hg38 | chr12 | 50,057,596 | 50,083,611 | 26,016 |
ENST00000228468.8 | hg19 | chr12 | 50,451,331 | 50,477,394 | 26,064 |
ENST00000447966.7 | hg19 | chr12 | 50,451,379 | 50,477,394 | 26,016 |
ENST00000552438.5 | hg19 | chr12 | 50,467,358 | 50,477,060 | 9,703 |
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