FHIP2B FHF complex subunit HOOK interacting protein 2B
Information
- Symbol
- FHIP2B
- Type
- protein-coding
- Description
- FHF complex subunit HOOK interacting protein 2B
- Entrez Gene ID
- 64760
- Genome
- hg19
- Position
- chr8:21,946,661-21,962,422
- Genome
- hg38
- Position
- chr8:22,089,150-22,104,911
- MIM
- 620230 OMIM
- HGNC
- HGNC:16492 HGNC
- Ensembl
- ENSG00000158863 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 14 |
Uncertain significance | 0 | 98 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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112 |
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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 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
---|---|
SYNONYM | FAI16 |
SYNONYM | FAM160B2 |
SYNONYM | RAI16 |
SYNONYM | RAM160B2 |
MIM | 620230 OMIM |
HGNC | HGNC:16492 HGNC |
Ensembl | ENSG00000158863 Ensembl |
AllianceGenome | HGNC:16492 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000289921.8 | hg38 | chr8 | 22,089,150 | 22,104,911 | 15,762 |
ENST00000289921.8 | hg19 | chr8 | 21,946,661 | 21,962,422 | 15,762 |
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