ZC3HC1 zinc finger C3HC-type containing 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 64 |
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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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 | HSPC216 |
SYNONYM | NIPA |
MIM | 619746 OMIM |
HGNC | HGNC:29913 HGNC |
Ensembl | ENSG00000091732 Ensembl |
AllianceGenome | HGNC:29913 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000358303.9 | hg38 | chr7 | 130,018,292 | 130,051,374 | 33,083 |
ENST00000714105.1 | hg38 | chr7 | 130,018,287 | 130,051,374 | 33,088 |
ENST00000481503.5 | hg38 | chr7 | 130,018,326 | 130,051,389 | 33,064 |
ENST00000360708.9 | hg38 | chr7 | 130,018,292 | 130,051,374 | 33,083 |
ENST00000358303.9 | hg19 | chr7 | 129,658,132 | 129,691,214 | 33,083 |
ENST00000360708.9 | hg19 | chr7 | 129,658,132 | 129,691,214 | 33,083 |
ENST00000714105.1 | hg19 | chr7 | 129,658,127 | 129,691,214 | 33,088 |
ENST00000481503.5 | hg19 | chr7 | 129,658,166 | 129,691,229 | 33,064 |
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