OCM oncomodulin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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 | OCM1 |
SYNONYM | OM |
SYNONYM | ONCM |
MIM | 164795 OMIM |
HGNC | HGNC:8105 HGNC |
Ensembl | ENSG00000122543 Ensembl |
AllianceGenome | HGNC:8105 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000416608.5 | hg38 | chr7 | 5,879,827 | 5,886,242 | 6,416 |
ENST00000242104.6 | hg38 | chr7 | 5,880,798 | 5,886,363 | 5,566 |
ENST00000416608.5 | hg19 | chr7 | 5,919,458 | 5,925,873 | 6,416 |
ENST00000242104.6 | hg19 | chr7 | 5,920,429 | 5,925,994 | 5,566 |
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