RNF32 ring finger protein 32
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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48 |
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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 | FKSG33 |
SYNONYM | HSD15 |
SYNONYM | LMBR2 |
MIM | 610241 OMIM |
HGNC | HGNC:17118 HGNC |
Ensembl | ENSG00000105982 Ensembl |
AllianceGenome | HGNC:17118 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000432459.6 | hg38 | chr7 | 156,640,747 | 156,677,124 | 36,378 |
ENST00000311822.12 | hg38 | chr7 | 156,640,879 | 156,677,130 | 36,252 |
ENST00000405335.5 | hg38 | chr7 | 156,640,784 | 156,677,095 | 36,312 |
ENST00000317955.10 | hg38 | chr7 | 156,640,774 | 156,677,130 | 36,357 |
ENST00000392743.6 | hg38 | chr7 | 156,642,977 | 156,677,124 | 34,148 |
ENST00000392741.6 | hg38 | chr7 | 156,643,790 | 156,660,350 | 16,561 |
ENST00000432459.6 | hg19 | chr7 | 156,433,441 | 156,469,818 | 36,378 |
ENST00000317955.10 | hg19 | chr7 | 156,433,468 | 156,469,824 | 36,357 |
ENST00000405335.5 | hg19 | chr7 | 156,433,478 | 156,469,789 | 36,312 |
ENST00000311822.12 | hg19 | chr7 | 156,433,573 | 156,469,824 | 36,252 |
ENST00000392743.6 | hg19 | chr7 | 156,435,671 | 156,469,818 | 34,148 |
ENST00000392741.6 | hg19 | chr7 | 156,436,484 | 156,453,044 | 16,561 |
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