GLS2 glutaminase 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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44 |
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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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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 |
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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 | GA |
SYNONYM | GLS |
SYNONYM | LGA |
SYNONYM | hLGA |
MIM | 606365 OMIM |
HGNC | HGNC:29570 HGNC |
Ensembl | ENSG00000135423 Ensembl |
AllianceGenome | HGNC:29570 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000311966.9 | hg38 | chr12 | 56,470,952 | 56,488,161 | 17,210 |
ENST00000610413.4 | hg38 | chr12 | 56,470,944 | 56,488,414 | 17,471 |
ENST00000623608.3 | hg38 | chr12 | 56,470,944 | 56,488,414 | 17,471 |
ENST00000539272.5 | hg38 | chr12 | 56,470,944 | 56,480,458 | 9,515 |
ENST00000539272.5 | hg19 | chr12 | 56,864,728 | 56,874,242 | 9,515 |
ENST00000311966.9 | hg19 | chr12 | 56,864,736 | 56,881,945 | 17,210 |
ENST00000623608.3 | hg19 | chr12 | 56,864,728 | 56,882,198 | 17,471 |
ENST00000610413.4 | hg19 | chr12 | 56,864,728 | 56,882,198 | 17,471 |
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