SLAMF8 SLAM family member 8
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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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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 | BLAME |
SYNONYM | CD353 |
SYNONYM | SBBI42 |
MIM | 606620 OMIM |
HGNC | HGNC:21391 HGNC |
Ensembl | ENSG00000158714 Ensembl |
AllianceGenome | HGNC:21391 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368104.4 | hg38 | chr1 | 159,826,811 | 159,835,679 | 8,869 |
ENST00000289707.10 | hg38 | chr1 | 159,826,873 | 159,837,492 | 10,620 |
ENST00000368104.4 | hg19 | chr1 | 159,796,601 | 159,805,469 | 8,869 |
ENST00000289707.10 | hg19 | chr1 | 159,796,663 | 159,807,282 | 10,620 |
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