WDR74 WD repeat domain 74
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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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
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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 |
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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 |
Type | ID |
---|---|
SYNONYM | Nsa1 |
MIM | 617947 OMIM |
HGNC | HGNC:25529 HGNC |
Ensembl | ENSG00000133316 Ensembl |
AllianceGenome | HGNC:25529 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000529106.5 | hg38 | chr11 | 62,832,912 | 62,840,156 | 7,245 |
ENST00000525239.5 | hg38 | chr11 | 62,832,912 | 62,841,809 | 8,898 |
ENST00000278856.9 | hg38 | chr11 | 62,832,911 | 62,839,590 | 6,680 |
ENST00000311713.11 | hg38 | chr11 | 62,832,911 | 62,839,581 | 6,671 |
ENST00000525752.5 | hg38 | chr11 | 62,832,952 | 62,840,380 | 7,429 |
ENST00000311713.11 | hg19 | chr11 | 62,600,383 | 62,607,053 | 6,671 |
ENST00000278856.9 | hg19 | chr11 | 62,600,383 | 62,607,062 | 6,680 |
ENST00000529106.5 | hg19 | chr11 | 62,600,384 | 62,607,628 | 7,245 |
ENST00000525239.5 | hg19 | chr11 | 62,600,384 | 62,609,281 | 8,898 |
ENST00000525752.5 | hg19 | chr11 | 62,600,424 | 62,607,852 | 7,429 |
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