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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C7orf24 |
| SYNONYM | CRF21 |
| SYNONYM | GCTG |
| SYNONYM | GGC |
| MIM | 137170 OMIM |
| HGNC | HGNC:21705 HGNC |
| Ensembl | ENSG00000006625 Ensembl |
| AllianceGenome | HGNC:21705 |
| Descrption | Source | Links |
|---|
| 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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