NPB neuropeptide B
Clinical Significance
MGeND | ClinVar | |
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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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20 |
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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 |
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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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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 | L7 |
SYNONYM | PPL7 |
SYNONYM | PPNPB |
MIM | 607996 OMIM |
HGNC | HGNC:30099 HGNC |
Ensembl | ENSG00000183979 Ensembl |
AllianceGenome | HGNC:30099 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000333383.8 | hg38 | chr17 | 81,902,238 | 81,902,905 | 668 |
ENST00000573081.1 | hg38 | chr17 | 81,900,745 | 81,902,898 | 2,154 |
ENST00000573081.1 | hg19 | chr17 | 79,858,621 | 79,860,774 | 2,154 |
ENST00000333383.8 | hg19 | chr17 | 79,860,114 | 79,860,781 | 668 |
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