ZNF121 zinc finger protein 121
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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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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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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 | D19S204 |
SYNONYM | ZHC32 |
SYNONYM | ZNF20 |
MIM | 194628 OMIM |
HGNC | HGNC:12904 HGNC |
Ensembl | ENSG00000197961 Ensembl |
AllianceGenome | HGNC:12904 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000586602.5 | hg38 | chr19 | 9,560,353 | 9,584,497 | 24,145 |
ENST00000320451.7 | hg38 | chr19 | 9,560,329 | 9,584,504 | 24,176 |
ENST00000320451.7 | hg19 | chr19 | 9,671,005 | 9,695,180 | 24,176 |
ENST00000586602.5 | hg19 | chr19 | 9,671,029 | 9,695,173 | 24,145 |
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