RNF6 ring finger protein 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Benign | 0 | 6 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 52 |
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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6 |
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 |
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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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MIM | 604242 OMIM |
HGNC | HGNC:10069 HGNC |
Ensembl | ENSG00000127870 Ensembl |
AllianceGenome | HGNC:10069 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000381588.9 | hg38 | chr13 | 26,212,775 | 26,222,314 | 9,540 |
ENST00000381570.7 | hg38 | chr13 | 26,212,775 | 26,221,703 | 8,929 |
ENST00000346166.7 | hg38 | chr13 | 26,212,762 | 26,221,842 | 9,081 |
ENST00000346166.7 | hg19 | chr13 | 26,786,899 | 26,795,979 | 9,081 |
ENST00000381570.7 | hg19 | chr13 | 26,786,912 | 26,795,840 | 8,929 |
ENST00000381588.9 | hg19 | chr13 | 26,786,912 | 26,796,451 | 9,540 |
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