ZNF415 zinc finger protein 415
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 76 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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80 |
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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 |
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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Search word | : | |
Filtering | : |
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 | Pact |
SYNONYM | ZfLp |
MIM | 619506 OMIM |
HGNC | HGNC:20636 HGNC |
Ensembl | ENSG00000170954 Ensembl |
AllianceGenome | HGNC:20636 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000243643.9 | hg38 | chr19 | 53,107,879 | 53,132,910 | 25,032 |
ENST00000500065.8 | hg38 | chr19 | 53,107,883 | 53,132,888 | 25,006 |
ENST00000595193.5 | hg38 | chr19 | 53,107,879 | 53,132,895 | 25,017 |
ENST00000599261.5 | hg38 | chr19 | 53,109,877 | 53,132,884 | 23,008 |
ENST00000597748.5 | hg38 | chr19 | 53,107,898 | 53,123,649 | 15,752 |
ENST00000601215.5 | hg38 | chr19 | 53,109,672 | 53,129,665 | 19,994 |
ENST00000600574.5 | hg38 | chr19 | 53,116,105 | 53,132,900 | 16,796 |
ENST00000601493.5 | hg38 | chr19 | 53,107,879 | 53,132,875 | 24,997 |
ENST00000597503.5 | hg38 | chr19 | 53,107,879 | 53,132,886 | 25,008 |
ENST00000594011.5 | hg38 | chr19 | 53,107,880 | 53,132,892 | 25,013 |
ENST00000421033.5 | hg38 | chr19 | 53,107,880 | 53,132,918 | 25,039 |
ENST00000595813.5 | hg38 | chr19 | 53,109,806 | 53,132,900 | 23,095 |
ENST00000597503.5 | hg19 | chr19 | 53,611,132 | 53,636,139 | 25,008 |
ENST00000595193.5 | hg19 | chr19 | 53,611,132 | 53,636,148 | 25,017 |
ENST00000243643.9 | hg19 | chr19 | 53,611,132 | 53,636,163 | 25,032 |
ENST00000594011.5 | hg19 | chr19 | 53,611,133 | 53,636,145 | 25,013 |
ENST00000421033.5 | hg19 | chr19 | 53,611,133 | 53,636,171 | 25,039 |
ENST00000500065.8 | hg19 | chr19 | 53,611,136 | 53,636,141 | 25,006 |
ENST00000597748.5 | hg19 | chr19 | 53,611,151 | 53,626,902 | 15,752 |
ENST00000600574.5 | hg19 | chr19 | 53,619,358 | 53,636,153 | 16,796 |
ENST00000595813.5 | hg19 | chr19 | 53,613,059 | 53,636,153 | 23,095 |
ENST00000599261.5 | hg19 | chr19 | 53,613,130 | 53,636,137 | 23,008 |
ENST00000601215.5 | hg19 | chr19 | 53,612,925 | 53,632,918 | 19,994 |
ENST00000601493.5 | hg19 | chr19 | 53,611,132 | 53,636,128 | 24,997 |
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