CD177 CD177 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 12 |
not provided | 1 | 0 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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82 |
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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
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 |
Search Word
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 | HNA-2a |
SYNONYM | HNA2A |
SYNONYM | NB1 |
SYNONYM | NB1 GP |
SYNONYM | PRV-1 |
SYNONYM | PRV1 |
MIM | 162860 OMIM |
HGNC | HGNC:30072 HGNC |
Ensembl | ENSG00000204936 Ensembl |
AllianceGenome | HGNC:30072 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000607855.5 | hg38 | chr19 | 43,353,691 | 43,354,525 | 835 |
ENST00000618265.5 | hg38 | chr19 | 43,353,686 | 43,363,172 | 9,487 |
ENST00000618265.5 | hg19 | chr19 | 43,857,838 | 43,867,324 | 9,487 |
ENST00000607855.5 | hg19 | chr19 | 43,857,843 | 43,858,677 | 835 |
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