FAM66E family with sequence similarity 66 member E
Information
- Symbol
- FAM66E
- Type
- ncRNA
- Description
- family with sequence similarity 66 member E
- Entrez Gene ID
- 100132103
- Genome
- hg19
- Position
- chr8:7,812,596-7,848,219
- Genome
- hg38
- Position
- chr8:7,955,074-7,990,697
- HGNC
- HGNC:18735 HGNC
- Ensembl
- ENSG00000225725 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 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 |
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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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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ENST00000533615.1 | hg38 | chr8 | 7,955,074 | 7,990,697 | 35,624 |
ENST00000529252.2 | hg38 | chr8 | 7,955,014 | 8,008,755 | 53,742 |
ENST00000529252.2 | hg19 | chr8 | 7,812,536 | 7,866,277 | 53,742 |
ENST00000533615.1 | hg19 | chr8 | 7,812,596 | 7,848,219 | 35,624 |
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