GGT6 gamma-glutamyltransferase 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 14 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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86 |
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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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MIM | 612341 OMIM |
HGNC | HGNC:26891 HGNC |
Ensembl | ENSG00000167741 Ensembl |
AllianceGenome | HGNC:26891 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000574154.5 | hg38 | chr17 | 4,557,312 | 4,560,818 | 3,507 |
ENST00000573591.1 | hg38 | chr17 | 4,557,820 | 4,559,935 | 2,116 |
ENST00000301395.7 | hg38 | chr17 | 4,556,927 | 4,560,581 | 3,655 |
ENST00000381550.8 | hg38 | chr17 | 4,556,927 | 4,560,577 | 3,651 |
ENST00000381550.8 | hg19 | chr17 | 4,460,222 | 4,463,872 | 3,651 |
ENST00000301395.7 | hg19 | chr17 | 4,460,222 | 4,463,876 | 3,655 |
ENST00000574154.5 | hg19 | chr17 | 4,460,607 | 4,464,113 | 3,507 |
ENST00000573591.1 | hg19 | chr17 | 4,461,115 | 4,463,230 | 2,116 |
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