ZNF155 zinc finger protein 155
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
not provided | 1 | 0 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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70 |
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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 | pHZ-96 |
MIM | 604086 OMIM |
HGNC | HGNC:12940 HGNC |
Ensembl | ENSG00000204920 Ensembl |
AllianceGenome | HGNC:12940 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000611002.4 | hg38 | chr19 | 43,984,170 | 43,998,325 | 14,156 |
ENST00000270014.7 | hg38 | chr19 | 43,984,188 | 43,998,326 | 14,139 |
ENST00000407951.6 | hg38 | chr19 | 43,984,194 | 43,997,853 | 13,660 |
ENST00000590615.5 | hg38 | chr19 | 43,984,217 | 43,997,554 | 13,338 |
ENST00000611002.4 | hg19 | chr19 | 44,488,322 | 44,502,477 | 14,156 |
ENST00000270014.7 | hg19 | chr19 | 44,488,340 | 44,502,478 | 14,139 |
ENST00000407951.6 | hg19 | chr19 | 44,488,346 | 44,502,005 | 13,660 |
ENST00000590615.5 | hg19 | chr19 | 44,488,369 | 44,501,706 | 13,338 |
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