CD6 CD6 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 24 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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96 |
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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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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 | TP120 |
MIM | 186720 OMIM |
HGNC | HGNC:1691 HGNC |
Ensembl | ENSG00000013725 Ensembl |
AllianceGenome | HGNC:1691 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000313421.11 | hg38 | chr11 | 60,971,680 | 61,020,377 | 48,698 |
ENST00000352009.9 | hg38 | chr11 | 60,971,866 | 61,019,321 | 47,456 |
ENST00000452451.6 | hg38 | chr11 | 60,971,866 | 61,019,321 | 47,456 |
ENST00000313421.11 | hg19 | chr11 | 60,739,152 | 60,787,849 | 48,698 |
ENST00000352009.9 | hg19 | chr11 | 60,739,338 | 60,786,793 | 47,456 |
ENST00000452451.6 | hg19 | chr11 | 60,739,338 | 60,786,793 | 47,456 |
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