CST11 cystatin 11
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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 |
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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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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 | CST8L |
SYNONYM | CTES2 |
SYNONYM | SC13 |
SYNONYM | dJ322G13.6 |
MIM | 609731 OMIM |
HGNC | HGNC:15959 HGNC |
Ensembl | ENSG00000125831 Ensembl |
AllianceGenome | HGNC:15959 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000377007.3 | hg38 | chr20 | 23,450,403 | 23,452,857 | 2,455 |
ENST00000377009.8 | hg38 | chr20 | 23,450,412 | 23,452,876 | 2,465 |
ENST00000377007.3 | hg19 | chr20 | 23,431,040 | 23,433,494 | 2,455 |
ENST00000377009.8 | hg19 | chr20 | 23,431,049 | 23,433,513 | 2,465 |
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