NBPF20 NBPF member 20
Clinical Significance
MGeND | ClinVar | |
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Likely benign | 0 | 1 |
Ranking
ClinVar | |
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0 |
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0 |
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1 |
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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
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 |
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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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MIM | 614007 OMIM |
HGNC | HGNC:32000 HGNC |
Ensembl | ENSG00000162825 Ensembl |
AllianceGenome | HGNC:32000 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000698833.1 | hg38 | chr1 | 145,290,005 | 145,425,603 | 135,599 |
ENST00000369373.9 | hg38 | chr1 | 145,289,900 | 145,405,567 | 115,668 |
ENST00000369190.5 | hg19 | chr1 | 144,146,808 | 144,160,564 | 13,757 |
ENST00000369372.4 | hg19 | chr1 | 144,151,520 | 144,205,836 | 54,317 |
ENST00000356801.6 | hg19 | chr1 | 144,173,162 | 144,213,129 | 39,968 |
ENST00000421555.2 | hg19 | chr1 | 144,215,387 | 144,219,425 | 4,039 |
ENST00000369373.5 | hg19 | chr1 | 144,220,127 | 144,224,192 | 4,066 |
Key | Value |
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strand | + |
start | 144,146,810 |
Gene Symbol | NBPF20 |
Entrez GeneId | 100,288,142 |
Chr Band | 1q21.2 |
end | 146,467,743 |
chr | chr1 |
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