RASA4 RAS p21 protein activator 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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 |
Type | ID |
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SYNONYM | CAPRI |
SYNONYM | GAPL |
MIM | 607943 OMIM |
HGNC | HGNC:23181 HGNC |
Ensembl | ENSG00000105808 Ensembl |
AllianceGenome | HGNC:23181 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000462172.5 | hg38 | chr7 | 102,582,691 | 102,616,729 | 34,039 |
ENST00000449970.6 | hg38 | chr7 | 102,582,325 | 102,616,756 | 34,432 |
ENST00000461209.5 | hg38 | chr7 | 102,582,323 | 102,611,591 | 29,269 |
ENST00000262940.12 | hg38 | chr7 | 102,579,646 | 102,616,756 | 37,111 |
ENST00000262940.12 | hg19 | chr7 | 102,220,093 | 102,257,203 | 37,111 |
ENST00000461209.5 | hg19 | chr7 | 102,222,770 | 102,252,038 | 29,269 |
ENST00000449970.6 | hg19 | chr7 | 102,222,772 | 102,257,203 | 34,432 |
ENST00000462172.5 | hg19 | chr7 | 102,223,138 | 102,257,176 | 34,039 |
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