FAM246B family with sequence similarity 246 member B
Information
- Symbol
- FAM246B
- Type
- protein-coding
- Description
- family with sequence similarity 246 member B
- Entrez Gene ID
- 117134597
- Genome
- hg19
- Position
- chr22:20,483,851-20,484,549
- Genome
- hg38
- Position
- chr22:18,633,984-18,634,682
- HGNC
- HGNC:54843 HGNC
- Ensembl
- ENSG00000286175 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 4 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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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
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000652395.1 | hg38 | chr22 | 18,633,984 | 18,634,682 | 699 |
ENST00000652395.1 | hg19 | chr22 | 20,483,851 | 20,484,549 | 699 |
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