COX7A1 cytochrome c oxidase subunit 7A1
Information
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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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 | COX7A |
SYNONYM | COX7AH |
SYNONYM | COX7AM |
MIM | 123995 OMIM |
HGNC | HGNC:2287 HGNC |
Ensembl | ENSG00000161281 Ensembl |
AllianceGenome | HGNC:2287 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000437291.6 | hg38 | chr19 | 36,150,922 | 36,152,025 | 1,104 |
ENST00000292907.8 | hg38 | chr19 | 36,150,922 | 36,152,447 | 1,526 |
ENST00000437291.6 | hg19 | chr19 | 36,641,824 | 36,642,927 | 1,104 |
ENST00000292907.8 | hg19 | chr19 | 36,641,824 | 36,643,349 | 1,526 |
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