CD244 CD244 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 10 |
risk factor | 0 | 2 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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42 |
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4 |
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 | 2B4 |
SYNONYM | NAIL |
SYNONYM | NKR2B4 |
SYNONYM | Nmrk |
SYNONYM | SLAMF4 |
MIM | 605554 OMIM |
HGNC | HGNC:18171 HGNC |
Ensembl | ENSG00000122223 Ensembl |
AllianceGenome | HGNC:18171 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000322302.7 | hg38 | chr1 | 160,831,271 | 160,862,700 | 31,430 |
ENST00000368034.9 | hg38 | chr1 | 160,830,160 | 160,862,887 | 32,728 |
ENST00000368033.7 | hg38 | chr1 | 160,831,183 | 160,862,760 | 31,578 |
ENST00000368034.9 | hg19 | chr1 | 160,799,950 | 160,832,677 | 32,728 |
ENST00000368033.7 | hg19 | chr1 | 160,800,973 | 160,832,550 | 31,578 |
ENST00000322302.7 | hg19 | chr1 | 160,801,061 | 160,832,490 | 31,430 |
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