NIBAN3 niban apoptosis regulator 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 98 |
Ranking
ClinVar | |
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0 |
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0 |
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108 |
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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 |
Prediction | |||||
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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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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 | BCNP1 |
SYNONYM | FAM129C |
MIM | 609967 OMIM |
HGNC | HGNC:24130 HGNC |
Ensembl | ENSG00000167483 Ensembl |
AllianceGenome | HGNC:24130 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000599124.1 | hg38 | chr19 | 17,527,304 | 17,552,024 | 24,721 |
ENST00000449408.6 | hg38 | chr19 | 17,527,278 | 17,553,634 | 26,357 |
ENST00000335393.8 | hg38 | chr19 | 17,523,301 | 17,553,839 | 30,539 |
ENST00000595684.5 | hg38 | chr19 | 17,523,301 | 17,549,811 | 26,511 |
ENST00000599164.6 | hg38 | chr19 | 17,527,267 | 17,553,640 | 26,374 |
ENST00000332386.9 | hg38 | chr19 | 17,523,301 | 17,552,026 | 28,726 |
ENST00000600871.5 | hg38 | chr19 | 17,527,291 | 17,551,960 | 24,670 |
ENST00000601861.5 | hg38 | chr19 | 17,527,238 | 17,553,639 | 26,402 |
ENST00000595684.5 | hg19 | chr19 | 17,634,110 | 17,660,620 | 26,511 |
ENST00000332386.9 | hg19 | chr19 | 17,634,110 | 17,662,835 | 28,726 |
ENST00000335393.8 | hg19 | chr19 | 17,634,110 | 17,664,648 | 30,539 |
ENST00000601861.5 | hg19 | chr19 | 17,638,047 | 17,664,448 | 26,402 |
ENST00000599164.6 | hg19 | chr19 | 17,638,076 | 17,664,449 | 26,374 |
ENST00000449408.6 | hg19 | chr19 | 17,638,087 | 17,664,443 | 26,357 |
ENST00000600871.5 | hg19 | chr19 | 17,638,100 | 17,662,769 | 24,670 |
ENST00000599124.1 | hg19 | chr19 | 17,638,113 | 17,662,833 | 24,721 |
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