ZCCHC2 zinc finger CCHC-type containing 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 20 |
Uncertain significance | 0 | 166 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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186 |
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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
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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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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 |
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MGeND data only
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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 | C18orf49 |
MIM | 620095 OMIM |
HGNC | HGNC:22916 HGNC |
Ensembl | ENSG00000141664 Ensembl |
AllianceGenome | HGNC:22916 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000269499.10 | hg38 | chr18 | 62,523,025 | 62,578,579 | 55,555 |
ENST00000586834.1 | hg38 | chr18 | 62,539,514 | 62,578,579 | 39,066 |
ENST00000269499.10 | hg19 | chr18 | 60,190,258 | 60,245,812 | 55,555 |
ENST00000586834.1 | hg19 | chr18 | 60,206,747 | 60,245,812 | 39,066 |
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