GNGT2 G protein subunit gamma transducin 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 3 | 0 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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6 |
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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 |
Search Word
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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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | HG3I |
SYNONYM | G-GAMMA-8 |
SYNONYM | G-GAMMA-C |
SYNONYM | GNG9 |
SYNONYM | GNGT8 |
MIM | 139391 OMIM |
HGNC | HGNC:4412 HGNC |
Ensembl | ENSG00000167083 Ensembl |
AllianceGenome | HGNC:4412 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000300406.6 | hg38 | chr17 | 49,206,389 | 49,209,385 | 2,997 |
ENST00000511277.5 | hg38 | chr17 | 49,206,229 | 49,209,400 | 3,172 |
ENST00000507680.6 | hg38 | chr17 | 49,206,237 | 49,210,574 | 4,338 |
ENST00000511673.1 | hg38 | chr17 | 49,206,757 | 49,209,400 | 2,644 |
ENST00000515635.5 | hg38 | chr17 | 49,206,579 | 49,209,217 | 2,639 |
ENST00000503070.5 | hg38 | chr17 | 49,202,791 | 49,208,912 | 6,122 |
ENST00000503070.5 | hg19 | chr17 | 47,280,153 | 47,286,274 | 6,122 |
ENST00000511277.5 | hg19 | chr17 | 47,283,591 | 47,286,762 | 3,172 |
ENST00000507680.6 | hg19 | chr17 | 47,283,599 | 47,287,936 | 4,338 |
ENST00000300406.6 | hg19 | chr17 | 47,283,751 | 47,286,747 | 2,997 |
ENST00000515635.5 | hg19 | chr17 | 47,283,941 | 47,286,579 | 2,639 |
ENST00000511673.1 | hg19 | chr17 | 47,284,119 | 47,286,762 | 2,644 |
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