RASAL1 RAS protein activator like 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 30 |
Uncertain significance | 0 | 114 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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4 |
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154 |
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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 | RASAL |
MIM | 604118 OMIM |
HGNC | HGNC:9873 HGNC |
Ensembl | ENSG00000111344 Ensembl |
AllianceGenome | HGNC:9873 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000261729.9 | hg38 | chr12 | 113,099,278 | 113,136,239 | 36,962 |
ENST00000548055.2 | hg38 | chr12 | 113,099,278 | 113,135,761 | 36,484 |
ENST00000446861.7 | hg38 | chr12 | 113,099,508 | 113,135,750 | 36,243 |
ENST00000546530.5 | hg38 | chr12 | 113,098,819 | 113,136,224 | 37,406 |
ENST00000546530.5 | hg19 | chr12 | 113,536,624 | 113,574,029 | 37,406 |
ENST00000548055.2 | hg19 | chr12 | 113,537,083 | 113,573,566 | 36,484 |
ENST00000261729.9 | hg19 | chr12 | 113,537,083 | 113,574,044 | 36,962 |
ENST00000446861.7 | hg19 | chr12 | 113,537,313 | 113,573,555 | 36,243 |
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