PEG3 paternally expressed 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 42 |
Likely benign | 0 | 54 |
Uncertain significance | 0 | 152 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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10 |
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232 |
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2 |
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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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 | PW1 |
SYNONYM | ZKSCAN22 |
SYNONYM | ZNF904 |
SYNONYM | ZSCAN24 |
MIM | 601483 OMIM |
HGNC | HGNC:8826 HGNC |
Ensembl | ENSG00000198300 Ensembl |
AllianceGenome | HGNC:8826 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000650632.1 | hg38 | chr19 | 56,810,918 | 56,840,726 | 29,809 |
ENST00000649680.1 | hg38 | chr19 | 56,810,121 | 56,840,726 | 30,606 |
ENST00000326441.15 | hg38 | chr19 | 56,810,082 | 56,840,726 | 30,645 |
ENST00000650102.1 | hg38 | chr19 | 56,811,081 | 56,840,726 | 29,646 |
ENST00000598410.5 | hg38 | chr19 | 56,813,148 | 56,840,726 | 27,579 |
ENST00000649428.1 | hg38 | chr19 | 56,810,187 | 56,837,818 | 27,632 |
ENST00000649233.1 | hg38 | chr19 | 56,810,102 | 56,840,728 | 30,627 |
ENST00000593695.5 | hg38 | chr19 | 56,813,675 | 56,840,696 | 27,022 |
ENST00000648694.1 | hg38 | chr19 | 56,810,077 | 56,840,726 | 30,650 |
ENST00000647621.1 | hg38 | chr19 | 56,812,819 | 56,840,726 | 27,908 |
ENST00000649735.1 | hg38 | chr19 | 56,812,158 | 56,840,661 | 28,504 |
ENST00000649876.1 | hg38 | chr19 | 56,810,121 | 56,840,726 | 30,606 |
ENST00000326441.15 | hg19 | chr19 | 57,321,450 | 57,352,094 | 30,645 |
ENST00000648694.1 | hg19 | chr19 | 57,321,445 | 57,352,094 | 30,650 |
ENST00000593695.5 | hg19 | chr19 | 57,325,043 | 57,352,064 | 27,022 |
ENST00000598410.5 | hg19 | chr19 | 57,324,516 | 57,352,094 | 27,579 |
ENST00000647621.1 | hg19 | chr19 | 57,324,187 | 57,352,094 | 27,908 |
ENST00000649233.1 | hg19 | chr19 | 57,321,470 | 57,352,096 | 30,627 |
ENST00000649428.1 | hg19 | chr19 | 57,321,555 | 57,349,186 | 27,632 |
ENST00000649735.1 | hg19 | chr19 | 57,323,526 | 57,352,029 | 28,504 |
ENST00000649876.1 | hg19 | chr19 | 57,321,489 | 57,352,094 | 30,606 |
ENST00000649680.1 | hg19 | chr19 | 57,321,489 | 57,352,094 | 30,606 |
ENST00000650102.1 | hg19 | chr19 | 57,322,449 | 57,352,094 | 29,646 |
ENST00000650632.1 | hg19 | chr19 | 57,322,286 | 57,352,094 | 29,809 |
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