POLR3G RNA polymerase III subunit G
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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
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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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 | C31 |
SYNONYM | RPC32 |
SYNONYM | RPC7 |
MIM | 617456 OMIM |
HGNC | HGNC:30075 HGNC |
Ensembl | ENSG00000113356 Ensembl |
AllianceGenome | HGNC:30075 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000504930.5 | hg38 | chr5 | 90,474,889 | 90,514,553 | 39,665 |
ENST00000651687.1 | hg38 | chr5 | 90,474,864 | 90,514,557 | 39,694 |
ENST00000514483.5 | hg38 | chr5 | 90,474,895 | 90,490,858 | 15,964 |
ENST00000651687.1 | hg19 | chr5 | 89,770,681 | 89,810,374 | 39,694 |
ENST00000504930.5 | hg19 | chr5 | 89,770,706 | 89,810,370 | 39,665 |
ENST00000514483.5 | hg19 | chr5 | 89,770,712 | 89,786,675 | 15,964 |
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