RNH1 ribonuclease/angiogenin inhibitor 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
risk factor | 0 | 8 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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68 |
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8 |
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 | IIAE12 |
SYNONYM | RAI |
SYNONYM | RNH |
MIM | 173320 OMIM |
HGNC | HGNC:10074 HGNC |
Ensembl | ENSG00000023191 Ensembl |
AllianceGenome | HGNC:10074 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000533410.5 | hg38 | chr11 | 494,546 | 507,218 | 12,673 |
ENST00000438658.6 | hg38 | chr11 | 494,548 | 506,785 | 12,238 |
ENST00000356187.9 | hg38 | chr11 | 494,561 | 507,300 | 12,740 |
ENST00000397614.5 | hg38 | chr11 | 494,513 | 506,821 | 12,309 |
ENST00000397615.6 | hg38 | chr11 | 494,515 | 506,800 | 12,286 |
ENST00000397604.7 | hg38 | chr11 | 494,515 | 507,253 | 12,739 |
ENST00000354420.7 | hg38 | chr11 | 494,515 | 507,242 | 12,728 |
ENST00000534797.5 | hg38 | chr11 | 494,512 | 503,570 | 9,059 |
ENST00000397614.5 | hg19 | chr11 | 494,513 | 506,821 | 12,309 |
ENST00000397615.6 | hg19 | chr11 | 494,515 | 506,800 | 12,286 |
ENST00000354420.7 | hg19 | chr11 | 494,515 | 507,242 | 12,728 |
ENST00000397604.7 | hg19 | chr11 | 494,515 | 507,253 | 12,739 |
ENST00000356187.9 | hg19 | chr11 | 494,561 | 507,300 | 12,740 |
ENST00000438658.6 | hg19 | chr11 | 494,548 | 506,785 | 12,238 |
ENST00000534797.5 | hg19 | chr11 | 494,512 | 503,570 | 9,059 |
ENST00000533410.5 | hg19 | chr11 | 494,546 | 507,218 | 12,673 |
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