SLAMF9 SLAM family member 9
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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36 |
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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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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 | CD2F-10 |
SYNONYM | CD2F10 |
SYNONYM | CD84-H1 |
SYNONYM | CD84H1 |
SYNONYM | SF2001 |
MIM | 608589 OMIM |
HGNC | HGNC:18430 HGNC |
Ensembl | ENSG00000162723 Ensembl |
AllianceGenome | HGNC:18430 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368092.7 | hg38 | chr1 | 159,951,492 | 159,954,220 | 2,729 |
ENST00000368093.4 | hg38 | chr1 | 159,951,492 | 159,954,237 | 2,746 |
ENST00000368092.7 | hg19 | chr1 | 159,921,282 | 159,924,010 | 2,729 |
ENST00000368093.4 | hg19 | chr1 | 159,921,282 | 159,924,027 | 2,746 |
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