DIRC3 disrupted in renal carcinoma 3
Clinical Significance
MGeND | ClinVar |
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Ranking
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 | 608262 OMIM |
HGNC | HGNC:17805 HGNC |
Ensembl | ENSG00000231672 Ensembl |
AllianceGenome | HGNC:17805 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000486365.5 | hg38 | chr2 | 217,319,167 | 217,756,593 | 437,427 |
ENST00000663562.1 | hg38 | chr2 | 217,284,057 | 217,624,581 | 340,525 |
ENST00000423123.1 | hg38 | chr2 | 217,703,900 | 217,756,555 | 52,656 |
ENST00000474063.5 | hg38 | chr2 | 217,284,019 | 217,599,932 | 315,914 |
ENST00000654616.2 | hg38 | chr2 | 217,284,023 | 217,336,618 | 52,596 |
ENST00000474063.5 | hg19 | chr2 | 218,148,742 | 218,464,655 | 315,914 |
ENST00000654616.2 | hg19 | chr2 | 218,148,746 | 218,201,341 | 52,596 |
ENST00000663562.1 | hg19 | chr2 | 218,148,780 | 218,489,304 | 340,525 |
ENST00000486365.5 | hg19 | chr2 | 218,183,890 | 218,621,316 | 437,427 |
ENST00000423123.1 | hg19 | chr2 | 218,568,623 | 218,621,278 | 52,656 |
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