COX6B2 cytochrome c oxidase subunit 6B2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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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
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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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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 | COXVIB2 |
SYNONYM | CT59 |
MIM | 618127 OMIM |
HGNC | HGNC:24380 HGNC |
Ensembl | ENSG00000160471 Ensembl |
AllianceGenome | HGNC:24380 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000326529.9 | hg38 | chr19 | 55,349,704 | 55,354,719 | 5,016 |
ENST00000588572.6 | hg38 | chr19 | 55,349,306 | 55,354,696 | 5,391 |
ENST00000590900.5 | hg38 | chr19 | 55,350,413 | 55,354,540 | 4,128 |
ENST00000593184.5 | hg38 | chr19 | 55,349,708 | 55,354,711 | 5,004 |
ENST00000589467.1 | hg38 | chr19 | 55,353,597 | 55,354,719 | 1,123 |
ENST00000588572.6 | hg19 | chr19 | 55,860,674 | 55,866,064 | 5,391 |
ENST00000326529.9 | hg19 | chr19 | 55,861,072 | 55,866,087 | 5,016 |
ENST00000593184.5 | hg19 | chr19 | 55,861,076 | 55,866,079 | 5,004 |
ENST00000590900.5 | hg19 | chr19 | 55,861,781 | 55,865,908 | 4,128 |
ENST00000589467.1 | hg19 | chr19 | 55,864,965 | 55,866,087 | 1,123 |
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