GPX5 glutathione peroxidase 5
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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2 |
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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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 |
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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 | EGLP |
SYNONYM | GPx-5 |
SYNONYM | GSHPx-5 |
SYNONYM | HEL-S-75p |
MIM | 603435 OMIM |
HGNC | HGNC:4557 HGNC |
Ensembl | ENSG00000224586 Ensembl |
AllianceGenome | HGNC:4557 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000412168.7 | hg38 | chr6 | 28,525,881 | 28,534,955 | 9,075 |
ENST00000469384.1 | hg38 | chr6 | 28,526,012 | 28,534,045 | 8,034 |
ENST00000412168.7 | hg19 | chr6 | 28,493,658 | 28,502,732 | 9,075 |
ENST00000469384.1 | hg19 | chr6 | 28,493,789 | 28,501,822 | 8,034 |
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