RUNDC3A RUN domain containing 3A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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 |
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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Filtering | : |
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 | RAP2IP |
SYNONYM | RPIP-8 |
SYNONYM | RPIP8 |
MIM | 605448 OMIM |
HGNC | HGNC:16984 HGNC |
Ensembl | ENSG00000108309 Ensembl |
AllianceGenome | HGNC:16984 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000225441.11 | hg38 | chr17 | 44,308,596 | 44,317,870 | 9,275 |
ENST00000590941.5 | hg38 | chr17 | 44,308,583 | 44,317,726 | 9,144 |
ENST00000426726.8 | hg38 | chr17 | 44,308,601 | 44,318,670 | 10,070 |
ENST00000590941.5 | hg19 | chr17 | 42,385,951 | 42,395,094 | 9,144 |
ENST00000225441.11 | hg19 | chr17 | 42,385,964 | 42,395,238 | 9,275 |
ENST00000426726.8 | hg19 | chr17 | 42,385,969 | 42,396,038 | 10,070 |
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