GARIN5B golgi associated RAB2 interactor family member 5B
Information
- Symbol
- GARIN5B
- Type
- protein-coding
- Description
- golgi associated RAB2 interactor family member 5B
- Entrez Gene ID
- 284418
- Genome
- hg19
- Position
- chr19:55,866,276-55,874,628
- Genome
- hg38
- Position
- chr19:55,354,908-55,363,260
- HGNC
- HGNC:25278 HGNC
- Ensembl
- ENSG00000180043 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 22 |
Uncertain significance | 0 | 154 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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176 |
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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 |
---|---|
SYNONYM | C19orf16 |
SYNONYM | FAM71E2 |
HGNC | HGNC:25278 HGNC |
Ensembl | ENSG00000180043 Ensembl |
AllianceGenome | HGNC:25278 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000424985.3 | hg38 | chr19 | 55,354,908 | 55,363,260 | 8,353 |
ENST00000424985.3 | hg19 | chr19 | 55,866,276 | 55,874,628 | 8,353 |
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