SLC8A2 solute carrier family 8 member A2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 16 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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80 |
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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 | NCX2 |
MIM | 601901 OMIM |
HGNC | HGNC:11069 HGNC |
Ensembl | ENSG00000118160 Ensembl |
AllianceGenome | HGNC:11069 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000236877.11 | hg38 | chr19 | 47,428,017 | 47,471,893 | 43,877 |
ENST00000542837.2 | hg38 | chr19 | 47,428,661 | 47,471,872 | 43,212 |
ENST00000236877.11 | hg19 | chr19 | 47,931,274 | 47,975,150 | 43,877 |
ENST00000542837.2 | hg19 | chr19 | 47,931,918 | 47,975,129 | 43,212 |
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