RANBP1 RAN binding protein 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 14 | 0 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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
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 |
Search Word
Target data | : |
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 | HTF9A |
MIM | 601180 OMIM |
HGNC | HGNC:9847 HGNC |
Ensembl | ENSG00000099901 Ensembl |
AllianceGenome | HGNC:9847 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000331821.8 | hg38 | chr22 | 20,117,505 | 20,127,355 | 9,851 |
ENST00000430524.6 | hg38 | chr22 | 20,116,104 | 20,127,355 | 11,252 |
ENST00000402752.5 | hg38 | chr22 | 20,117,424 | 20,127,355 | 9,932 |
ENST00000430524.6 | hg19 | chr22 | 20,103,627 | 20,114,878 | 11,252 |
ENST00000402752.5 | hg19 | chr22 | 20,104,947 | 20,114,878 | 9,932 |
ENST00000331821.8 | hg19 | chr22 | 20,105,028 | 20,114,878 | 9,851 |
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