GSTM2 glutathione S-transferase mu 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 8 |
not provided | 1 | 0 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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
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 | GST4 |
SYNONYM | GSTM |
SYNONYM | GSTM2-2 |
SYNONYM | GTHMUS |
MIM | 138380 OMIM |
HGNC | HGNC:4634 HGNC |
Ensembl | ENSG00000213366 Ensembl |
AllianceGenome | HGNC:4634 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000241337.9 | hg38 | chr1 | 109,668,057 | 109,675,286 | 7,230 |
ENST00000460717.8 | hg38 | chr1 | 109,668,051 | 109,709,549 | 41,499 |
ENST00000442650.5 | hg38 | chr1 | 109,668,022 | 109,683,997 | 15,976 |
ENST00000369831.6 | hg38 | chr1 | 109,668,022 | 109,709,549 | 41,528 |
ENST00000369829.2 | hg38 | chr1 | 109,668,092 | 109,673,525 | 5,434 |
ENST00000369827.7 | hg38 | chr1 | 109,668,036 | 109,675,283 | 7,248 |
ENST00000414179.6 | hg38 | chr1 | 109,668,088 | 109,683,584 | 15,497 |
ENST00000442650.5 | hg19 | chr1 | 110,210,644 | 110,226,619 | 15,976 |
ENST00000369831.6 | hg19 | chr1 | 110,210,644 | 110,252,171 | 41,528 |
ENST00000369827.7 | hg19 | chr1 | 110,210,658 | 110,217,905 | 7,248 |
ENST00000460717.8 | hg19 | chr1 | 110,210,673 | 110,252,171 | 41,499 |
ENST00000241337.9 | hg19 | chr1 | 110,210,679 | 110,217,908 | 7,230 |
ENST00000414179.6 | hg19 | chr1 | 110,210,710 | 110,226,206 | 15,497 |
ENST00000369829.2 | hg19 | chr1 | 110,210,714 | 110,216,147 | 5,434 |
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