NABP1 nucleic acid binding protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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 |
Search Word
Target data | : |
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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Search word | : | |
Filtering | : |
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 | NABP1-OT1 |
SYNONYM | OBFC2A |
SYNONYM | SOSS-B2 |
SYNONYM | SSB2 |
MIM | 612103 OMIM |
HGNC | HGNC:26232 HGNC |
Ensembl | ENSG00000173559 Ensembl |
AllianceGenome | HGNC:26232 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000410026.7 | hg38 | chr2 | 191,678,136 | 191,696,662 | 18,527 |
ENST00000425611.9 | hg38 | chr2 | 191,678,136 | 191,686,943 | 8,808 |
ENST00000409510.5 | hg38 | chr2 | 191,678,204 | 191,685,894 | 7,691 |
ENST00000425611.9 | hg19 | chr2 | 192,542,862 | 192,551,669 | 8,808 |
ENST00000410026.7 | hg19 | chr2 | 192,542,862 | 192,561,388 | 18,527 |
ENST00000409510.5 | hg19 | chr2 | 192,542,930 | 192,550,620 | 7,691 |
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