ZNF480 zinc finger protein 480
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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56 |
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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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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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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 | 613910 OMIM |
HGNC | HGNC:23305 HGNC |
Ensembl | ENSG00000198464 Ensembl |
AllianceGenome | HGNC:23305 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000490272.1 | hg38 | chr19 | 52,297,179 | 52,323,680 | 26,502 |
ENST00000595962.6 | hg38 | chr19 | 52,297,169 | 52,325,922 | 28,754 |
ENST00000335090.6 | hg38 | chr19 | 52,300,394 | 52,324,080 | 23,687 |
ENST00000334564.11 | hg38 | chr19 | 52,297,179 | 52,323,158 | 25,980 |
ENST00000595962.6 | hg19 | chr19 | 52,800,422 | 52,829,175 | 28,754 |
ENST00000334564.11 | hg19 | chr19 | 52,800,432 | 52,826,411 | 25,980 |
ENST00000490272.1 | hg19 | chr19 | 52,800,432 | 52,826,933 | 26,502 |
ENST00000335090.6 | hg19 | chr19 | 52,803,647 | 52,827,333 | 23,687 |
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