ZNF101 zinc finger protein 101
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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52 |
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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 |
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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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SYNONYM | HZF12 |
MIM | 603983 OMIM |
HGNC | HGNC:12881 HGNC |
Ensembl | ENSG00000181896 Ensembl |
AllianceGenome | HGNC:12881 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000415784.6 | hg38 | chr19 | 19,668,901 | 19,680,329 | 11,429 |
ENST00000592502.2 | hg38 | chr19 | 19,668,839 | 19,683,506 | 14,668 |
ENST00000444249.6 | hg38 | chr19 | 19,668,851 | 19,680,032 | 11,182 |
ENST00000592502.2 | hg19 | chr19 | 19,779,648 | 19,794,315 | 14,668 |
ENST00000444249.6 | hg19 | chr19 | 19,779,660 | 19,790,841 | 11,182 |
ENST00000415784.6 | hg19 | chr19 | 19,779,710 | 19,791,138 | 11,429 |
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