CD83 CD83 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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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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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | BL11 |
SYNONYM | HB15 |
MIM | 604534 OMIM |
HGNC | HGNC:1703 HGNC |
Ensembl | ENSG00000112149 Ensembl |
AllianceGenome | HGNC:1703 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000612003.4 | hg38 | chr6 | 14,117,256 | 14,136,918 | 19,663 |
ENST00000379153.4 | hg38 | chr6 | 14,117,772 | 14,136,906 | 19,135 |
ENST00000612003.4 | hg19 | chr6 | 14,117,487 | 14,137,149 | 19,663 |
ENST00000379153.4 | hg19 | chr6 | 14,118,003 | 14,137,137 | 19,135 |
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