IRS4 insulin receptor substrate 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely pathogenic | 0 | 6 |
Benign | 0 | 18 |
Likely benign | 0 | 30 |
not provided | 6 | 0 |
Uncertain significance | 0 | 122 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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170 |
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6 |
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 |
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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 | CHNG9 |
SYNONYM | IRS-4 |
SYNONYM | PY160 |
MIM | 300904 OMIM |
HGNC | HGNC:6128 HGNC |
Ensembl | ENSG00000133124 Ensembl |
AllianceGenome | HGNC:6128 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000372129.4 | hg38 | chrX | 108,719,946 | 108,736,563 | 16,618 |
ENST00000564206.2 | hg38 | chrX | 108,719,949 | 108,736,409 | 16,461 |
ENST00000372129.4 | hg19 | chrX | 107,963,176 | 107,979,793 | 16,618 |
ENST00000564206.2 | hg19 | chrX | 107,963,179 | 107,979,639 | 16,461 |
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