FAM246C family with sequence similarity 246 member C (gene/pseudogene)
Information
- Symbol
- FAM246C
- Type
- protein-coding
- Description
- family with sequence similarity 246 member C (gene/pseudogene)
- Entrez Gene ID
- 117134596
- Genome
- hg19
- Position
- chr22:19,017,037-19,018,755
- Genome
- hg38
- Position
- chr22:19,029,524-19,031,242
- HGNC
- HGNC:54842 HGNC
- Ensembl
- ENSG00000286025 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 14 | 0 |
Ranking
ClinVar | |
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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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
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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Search word | : | |
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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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ENST00000652053.1 | hg38 | chr22 | 19,029,524 | 19,031,242 | 1,719 |
ENST00000697771.1 | hg38 | chr22 | 19,029,524 | 19,031,208 | 1,685 |
ENST00000697771.1 | hg19 | chr22 | 19,017,037 | 19,018,721 | 1,685 |
ENST00000652053.1 | hg19 | chr22 | 19,017,037 | 19,018,755 | 1,719 |
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