CD81 CD81 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 60 |
Likely benign | 0 | 232 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 174 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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38 |
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422 |
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2 |
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 | CVID6 |
SYNONYM | S5.7 |
SYNONYM | TAPA1 |
SYNONYM | TSPAN28 |
MIM | 186845 OMIM |
HGNC | HGNC:1701 HGNC |
Ensembl | ENSG00000110651 Ensembl |
AllianceGenome | HGNC:1701 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000492627.5 | hg38 | chr11 | 2,382,460 | 2,397,016 | 14,557 |
ENST00000533417.6 | hg38 | chr11 | 2,378,931 | 2,397,382 | 18,452 |
ENST00000475945.7 | hg38 | chr11 | 2,376,177 | 2,397,802 | 21,626 |
ENST00000263645.10 | hg38 | chr11 | 2,377,310 | 2,397,397 | 20,088 |
ENST00000526072.5 | hg38 | chr11 | 2,390,095 | 2,397,304 | 7,210 |
ENST00000381036.7 | hg38 | chr11 | 2,386,057 | 2,396,916 | 10,860 |
ENST00000481687.1 | hg38 | chr11 | 2,393,848 | 2,396,979 | 3,132 |
ENST00000475945.7 | hg19 | chr11 | 2,397,407 | 2,419,032 | 21,626 |
ENST00000263645.10 | hg19 | chr11 | 2,398,540 | 2,418,627 | 20,088 |
ENST00000381036.7 | hg19 | chr11 | 2,407,287 | 2,418,146 | 10,860 |
ENST00000481687.1 | hg19 | chr11 | 2,415,078 | 2,418,209 | 3,132 |
ENST00000492627.5 | hg19 | chr11 | 2,403,690 | 2,418,246 | 14,557 |
ENST00000526072.5 | hg19 | chr11 | 2,411,325 | 2,418,534 | 7,210 |
ENST00000533417.6 | hg19 | chr11 | 2,400,161 | 2,418,612 | 18,452 |
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