SLAMF6 SLAM family member 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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 | CD352 |
SYNONYM | KALI |
SYNONYM | KALIb |
SYNONYM | Ly108 |
SYNONYM | NTB-A |
SYNONYM | NTBA |
SYNONYM | SF2000 |
MIM | 606446 OMIM |
HGNC | HGNC:21392 HGNC |
Ensembl | ENSG00000162739 Ensembl |
AllianceGenome | HGNC:21392 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000368059.7 | hg38 | chr1 | 160,485,030 | 160,523,262 | 38,233 |
ENST00000368057.8 | hg38 | chr1 | 160,485,036 | 160,523,255 | 38,220 |
ENST00000368055.1 | hg38 | chr1 | 160,486,693 | 160,523,242 | 36,550 |
ENST00000368059.7 | hg19 | chr1 | 160,454,820 | 160,493,052 | 38,233 |
ENST00000368057.8 | hg19 | chr1 | 160,454,826 | 160,493,045 | 38,220 |
ENST00000368055.1 | hg19 | chr1 | 160,456,483 | 160,493,032 | 36,550 |
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