NECTIN2 nectin cell adhesion molecule 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 18 |
Likely benign | 0 | 40 |
not provided | 11 | 0 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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6 |
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62 |
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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
Search Word
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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Category | : |
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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 | CD112 |
SYNONYM | HVEB |
SYNONYM | PRR2 |
SYNONYM | PVRL2 |
SYNONYM | PVRR2 |
MIM | 600798 OMIM |
HGNC | HGNC:9707 HGNC |
Ensembl | ENSG00000130202 Ensembl |
AllianceGenome | HGNC:9707 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000252483.10 | hg38 | chr19 | 44,846,297 | 44,889,223 | 42,927 |
ENST00000252485.8 | hg38 | chr19 | 44,846,175 | 44,878,941 | 32,767 |
ENST00000252485.8 | hg19 | chr19 | 45,349,432 | 45,382,198 | 32,767 |
ENST00000252483.10 | hg19 | chr19 | 45,349,554 | 45,392,480 | 42,927 |
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