PYY peptide YY
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 4 |
Benign | 0 | 18 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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46 |
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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
[No Data.]
Locus Zoom
Variants
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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 | PYY-I |
SYNONYM | PYY1 |
MIM | 600781 OMIM |
HGNC | HGNC:9748 HGNC |
Ensembl | ENSG00000131096 Ensembl |
AllianceGenome | HGNC:9748 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000360085.6 | hg38 | chr17 | 43,952,738 | 44,004,469 | 51,732 |
ENST00000592796.2 | hg38 | chr17 | 43,952,741 | 43,953,940 | 1,200 |
ENST00000692052.1 | hg38 | chr17 | 43,952,733 | 43,953,940 | 1,208 |
ENST00000692052.1 | hg19 | chr17 | 42,030,101 | 42,031,308 | 1,208 |
ENST00000360085.6 | hg19 | chr17 | 42,030,106 | 42,081,837 | 51,732 |
ENST00000592796.2 | hg19 | chr17 | 42,030,109 | 42,031,308 | 1,200 |
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