RASL10A RAS like family 10 member A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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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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 |
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SYNONYM | RRP22 |
MIM | 602220 OMIM |
HGNC | HGNC:16954 HGNC |
Ensembl | ENSG00000100276 Ensembl |
AllianceGenome | HGNC:16954 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000401450.3 | hg38 | chr22 | 29,312,933 | 29,315,692 | 2,760 |
ENST00000216101.7 | hg38 | chr22 | 29,312,933 | 29,315,697 | 2,765 |
ENST00000401450.3 | hg19 | chr22 | 29,708,922 | 29,711,681 | 2,760 |
ENST00000216101.7 | hg19 | chr22 | 29,708,922 | 29,711,686 | 2,765 |
Key | Value |
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strand | - |
UniProt | TSG |
start | 29,708,921 |
Gene Symbol | RASL10A |
Entrez GeneId | 10,633 |
Chr Band | 22q12.2 |
end | 29,711,744 |
chr | chr22 |
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