RND3 Rho family GTPase 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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
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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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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 |
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SYNONYM | ARHE |
SYNONYM | Rho8 |
SYNONYM | RhoE |
SYNONYM | memB |
MIM | 602924 OMIM |
HGNC | HGNC:671 HGNC |
Ensembl | ENSG00000115963 Ensembl |
AllianceGenome | HGNC:671 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000409557.5 | hg38 | chr2 | 150,468,209 | 150,485,382 | 17,174 |
ENST00000375734.6 | hg38 | chr2 | 150,468,195 | 150,487,667 | 19,473 |
ENST00000263895.9 | hg38 | chr2 | 150,468,195 | 150,487,667 | 19,473 |
ENST00000375734.6 | hg19 | chr2 | 151,324,709 | 151,344,181 | 19,473 |
ENST00000263895.9 | hg19 | chr2 | 151,324,709 | 151,344,181 | 19,473 |
ENST00000409557.5 | hg19 | chr2 | 151,324,723 | 151,341,896 | 17,174 |
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