EGR4 early growth response 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 80 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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96 |
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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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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 |
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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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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 | AT133 |
SYNONYM | NGFI-C |
SYNONYM | NGFIC |
SYNONYM | PAT133 |
MIM | 128992 OMIM |
HGNC | HGNC:3241 HGNC |
Ensembl | ENSG00000135625 Ensembl |
AllianceGenome | HGNC:3241 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000545030.1 | hg38 | chr2 | 73,290,930 | 73,293,701 | 2,772 |
ENST00000436467.4 | hg38 | chr2 | 73,290,929 | 73,293,548 | 2,620 |
ENST00000436467.4 | hg19 | chr2 | 73,518,057 | 73,520,676 | 2,620 |
ENST00000545030.1 | hg19 | chr2 | 73,518,058 | 73,520,829 | 2,772 |
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