DNAAF10 dynein axonemal assembly factor 10
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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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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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 | WDR92 |
MIM | 610729 OMIM |
HGNC | HGNC:25176 HGNC |
Ensembl | ENSG00000243667 Ensembl |
AllianceGenome | HGNC:25176 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000406245.6 | hg38 | chr2 | 68,134,084 | 68,157,473 | 23,390 |
ENST00000409164.1 | hg38 | chr2 | 68,134,090 | 68,157,482 | 23,393 |
ENST00000295121.11 | hg38 | chr2 | 68,129,805 | 68,157,527 | 27,723 |
ENST00000295121.11 | hg19 | chr2 | 68,356,937 | 68,384,659 | 27,723 |
ENST00000406245.6 | hg19 | chr2 | 68,361,216 | 68,384,605 | 23,390 |
ENST00000409164.1 | hg19 | chr2 | 68,361,222 | 68,384,614 | 23,393 |
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