FAM90A15 family with sequence similarity 90 member A15
Information
- Symbol
- FAM90A15
- Type
- protein-coding
- Description
- family with sequence similarity 90 member A15
- Entrez Gene ID
- 389630
- Genome
- hg19
- Position
- chr8:7,114,426-7,117,436
- Genome
- hg38
- Position
- chr8:7,256,904-7,259,914
- MIM
- 613051 OMIM
- HGNC
- HGNC:32263 HGNC
- Ensembl
- ENSG00000230045 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
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not provided | 1 | 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 |
Type | ID |
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SYNONYM | FAM90A15P |
MIM | 613051 OMIM |
HGNC | HGNC:32263 HGNC |
Ensembl | ENSG00000230045 Ensembl |
AllianceGenome | HGNC:32263 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000514465.1 | hg38 | chr8 | 7,256,904 | 7,259,914 | 3,011 |
ENST00000514465.1 | hg19 | chr8 | 7,114,426 | 7,117,436 | 3,011 |
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