FAM187B family with sequence similarity 187 member B
Information
- Symbol
- FAM187B
- Type
- protein-coding
- Description
- family with sequence similarity 187 member B
- Entrez Gene ID
- 148109
- Genome
- hg19
- Position
- chr19:35,715,703-35,719,642
- Genome
- hg38
- Position
- chr19:35,224,800-35,228,739
- HGNC
- HGNC:26366 HGNC
- Ensembl
- ENSG00000177558 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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72 |
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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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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 | TMEM162 |
HGNC | HGNC:26366 HGNC |
Ensembl | ENSG00000177558 Ensembl |
AllianceGenome | HGNC:26366 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000324675.4 | hg38 | chr19 | 35,224,800 | 35,228,739 | 3,940 |
ENST00000324675.4 | hg19 | chr19 | 35,715,703 | 35,719,642 | 3,940 |
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