ZNF45 zinc finger protein 45
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 84 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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86 |
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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
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 |
Search Word
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 | KOX5 |
SYNONYM | ZNF13 |
MIM | 194554 OMIM |
HGNC | HGNC:13111 HGNC |
Ensembl | ENSG00000124459 Ensembl |
AllianceGenome | HGNC:13111 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000615985.4 | hg38 | chr19 | 43,912,631 | 43,924,312 | 11,682 |
ENST00000589703.5 | hg38 | chr19 | 43,913,129 | 43,922,287 | 9,159 |
ENST00000269973.10 | hg38 | chr19 | 43,912,624 | 43,935,282 | 22,659 |
ENST00000269973.10 | hg19 | chr19 | 44,416,776 | 44,439,434 | 22,659 |
ENST00000615985.4 | hg19 | chr19 | 44,416,783 | 44,428,464 | 11,682 |
ENST00000589703.5 | hg19 | chr19 | 44,417,281 | 44,426,439 | 9,159 |
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