POMC proopiomelanocortin
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 28 |
Likely pathogenic | 0 | 8 |
Benign | 0 | 16 |
Likely benign | 0 | 46 |
Conflicting classifications of pathogenicity | 0 | 22 |
not provided | 2 | 0 |
Uncertain significance | 0 | 138 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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52 |
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168 |
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12 |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
---|---|
SYNONYM | ACTH |
SYNONYM | CLIP |
SYNONYM | LPH |
SYNONYM | MSH |
SYNONYM | NPP |
SYNONYM | OBAIRH |
SYNONYM | POC |
MIM | 176830 OMIM |
HGNC | HGNC:9201 HGNC |
Ensembl | ENSG00000115138 Ensembl |
AllianceGenome | HGNC:9201 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000380794.5 | hg38 | chr2 | 25,160,853 | 25,168,690 | 7,838 |
ENST00000395826.7 | hg38 | chr2 | 25,160,860 | 25,168,580 | 7,721 |
ENST00000405623.5 | hg38 | chr2 | 25,160,915 | 25,168,903 | 7,989 |
ENST00000264708.7 | hg38 | chr2 | 25,160,985 | 25,168,571 | 7,587 |
ENST00000380794.5 | hg19 | chr2 | 25,383,722 | 25,391,559 | 7,838 |
ENST00000395826.7 | hg19 | chr2 | 25,383,729 | 25,391,449 | 7,721 |
ENST00000405623.5 | hg19 | chr2 | 25,383,784 | 25,391,772 | 7,989 |
ENST00000264708.7 | hg19 | chr2 | 25,383,854 | 25,391,440 | 7,587 |
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