GGCT gamma-glutamylcyclotransferase
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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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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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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 | C7orf24 |
SYNONYM | CRF21 |
SYNONYM | GCTG |
SYNONYM | GGC |
MIM | 137170 OMIM |
HGNC | HGNC:21705 HGNC |
Ensembl | ENSG00000006625 Ensembl |
AllianceGenome | HGNC:21705 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409144.5 | hg38 | chr7 | 30,496,633 | 30,504,801 | 8,169 |
ENST00000005374.10 | hg38 | chr7 | 30,496,623 | 30,504,841 | 8,219 |
ENST00000409390.5 | hg38 | chr7 | 30,497,002 | 30,504,799 | 7,798 |
ENST00000409436.2 | hg38 | chr7 | 30,497,473 | 30,504,816 | 7,344 |
ENST00000275428.9 | hg38 | chr7 | 30,496,621 | 30,504,829 | 8,209 |
ENST00000275428.9 | hg19 | chr7 | 30,536,237 | 30,544,445 | 8,209 |
ENST00000005374.10 | hg19 | chr7 | 30,536,239 | 30,544,457 | 8,219 |
ENST00000409144.5 | hg19 | chr7 | 30,536,249 | 30,544,417 | 8,169 |
ENST00000409390.5 | hg19 | chr7 | 30,536,618 | 30,544,415 | 7,798 |
ENST00000409436.2 | hg19 | chr7 | 30,537,089 | 30,544,432 | 7,344 |
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