MGST1 microsomal glutathione S-transferase 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
association | 0 | 4 |
protective | 0 | 4 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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8 |
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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Target data | : |
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 | GST12 |
SYNONYM | MGST |
SYNONYM | MGST-I |
SYNONYM | PMAN |
MIM | 138330 OMIM |
HGNC | HGNC:7061 HGNC |
Ensembl | ENSG00000008394 Ensembl |
AllianceGenome | HGNC:7061 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000396210.8 | hg38 | chr12 | 16,347,645 | 16,364,410 | 16,766 |
ENST00000396207.1 | hg38 | chr12 | 16,353,417 | 16,364,409 | 10,993 |
ENST00000396209.5 | hg38 | chr12 | 16,347,778 | 16,364,409 | 16,632 |
ENST00000540056.5 | hg38 | chr12 | 16,347,778 | 16,364,071 | 16,294 |
ENST00000010404.6 | hg38 | chr12 | 16,347,142 | 16,364,409 | 17,268 |
ENST00000535309.5 | hg38 | chr12 | 16,347,694 | 16,377,192 | 29,499 |
ENST00000010404.6 | hg19 | chr12 | 16,500,076 | 16,517,343 | 17,268 |
ENST00000396207.1 | hg19 | chr12 | 16,506,351 | 16,517,343 | 10,993 |
ENST00000396209.5 | hg19 | chr12 | 16,500,712 | 16,517,343 | 16,632 |
ENST00000396210.8 | hg19 | chr12 | 16,500,579 | 16,517,344 | 16,766 |
ENST00000535309.5 | hg19 | chr12 | 16,500,628 | 16,530,126 | 29,499 |
ENST00000540056.5 | hg19 | chr12 | 16,500,712 | 16,517,005 | 16,294 |
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