RFC5 replication factor C subunit 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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 | RFC36 |
MIM | 600407 OMIM |
HGNC | HGNC:9973 HGNC |
Ensembl | ENSG00000111445 Ensembl |
AllianceGenome | HGNC:9973 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000392542.6 | hg38 | chr12 | 118,016,722 | 118,032,234 | 15,513 |
ENST00000454402.7 | hg38 | chr12 | 118,016,703 | 118,032,234 | 15,532 |
ENST00000454402.7 | hg19 | chr12 | 118,454,508 | 118,470,039 | 15,532 |
ENST00000392542.6 | hg19 | chr12 | 118,454,527 | 118,470,039 | 15,513 |
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