NABP2 nucleic acid binding protein 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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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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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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 | OBFC2B |
SYNONYM | SOSS-B1 |
SYNONYM | SSB1 |
SYNONYM | hSSB1 |
MIM | 612104 OMIM |
HGNC | HGNC:28412 HGNC |
Ensembl | ENSG00000139579 Ensembl |
AllianceGenome | HGNC:28412 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000341463.5 | hg38 | chr12 | 56,224,401 | 56,229,844 | 5,444 |
ENST00000267023.9 | hg38 | chr12 | 56,224,342 | 56,229,854 | 5,513 |
ENST00000380198.6 | hg38 | chr12 | 56,224,359 | 56,229,854 | 5,496 |
ENST00000267023.9 | hg19 | chr12 | 56,618,126 | 56,623,638 | 5,513 |
ENST00000380198.6 | hg19 | chr12 | 56,618,143 | 56,623,638 | 5,496 |
ENST00000341463.5 | hg19 | chr12 | 56,618,185 | 56,623,628 | 5,444 |
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