CFAP68 cilia and flagella associated protein 68
Information
- Symbol
- CFAP68
- Type
- protein-coding
- Description
- cilia and flagella associated protein 68
- Entrez Gene ID
- 64776
- Genome
- hg19
- Position
- chr11:111,750,265-111,756,699
- Genome
- hg38
- Position
- chr11:111,879,541-111,885,975
- HGNC
- HGNC:1163 HGNC
- Ensembl
- ENSG00000137720 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
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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 |
Prediction | |||||
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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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Category | : |
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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 |
---|---|---|---|---|---|
ENST00000528125.5 | hg38 | chr11 | 111,878,935 | 111,883,900 | 4,966 |
ENST00000529270.1 | hg38 | chr11 | 111,880,776 | 111,884,069 | 3,294 |
ENST00000530214.5 | hg38 | chr11 | 111,879,542 | 111,884,074 | 4,533 |
ENST00000260276.8 | hg38 | chr11 | 111,879,541 | 111,885,975 | 6,435 |
ENST00000528125.5 | hg19 | chr11 | 111,749,659 | 111,754,624 | 4,966 |
ENST00000260276.8 | hg19 | chr11 | 111,750,265 | 111,756,699 | 6,435 |
ENST00000530214.5 | hg19 | chr11 | 111,750,266 | 111,754,798 | 4,533 |
ENST00000529270.1 | hg19 | chr11 | 111,751,500 | 111,754,793 | 3,294 |
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