CD4 CD4 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Benign | 14 | 36 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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18 |
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54 |
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4 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 | |||||
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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 | CD4mut |
SYNONYM | IMD79 |
SYNONYM | Leu-3 |
SYNONYM | OKT4D |
SYNONYM | T4 |
MIM | 186940 OMIM |
HGNC | HGNC:1678 HGNC |
Ensembl | ENSG00000010610 Ensembl |
AllianceGenome | HGNC:1678 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000011653.9 | hg38 | chr12 | 6,789,528 | 6,820,799 | 31,272 |
ENST00000541982.5 | hg38 | chr12 | 6,789,536 | 6,816,281 | 26,746 |
ENST00000011653.9 | hg19 | chr12 | 6,898,694 | 6,929,965 | 31,272 |
ENST00000541982.5 | hg19 | chr12 | 6,898,702 | 6,925,447 | 26,746 |
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