IAPP islet amyloid polypeptide
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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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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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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 | DAP |
SYNONYM | IAP |
MIM | 147940 OMIM |
HGNC | HGNC:5329 HGNC |
Ensembl | ENSG00000121351 Ensembl |
AllianceGenome | HGNC:5329 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000542023.1 | hg38 | chr12 | 21,372,919 | 21,379,978 | 7,060 |
ENST00000240652.8 | hg38 | chr12 | 21,372,902 | 21,379,980 | 7,079 |
ENST00000539393.5 | hg38 | chr12 | 21,354,959 | 21,378,495 | 23,537 |
ENST00000539393.5 | hg19 | chr12 | 21,507,893 | 21,531,429 | 23,537 |
ENST00000240652.8 | hg19 | chr12 | 21,525,836 | 21,532,914 | 7,079 |
ENST00000542023.1 | hg19 | chr12 | 21,525,853 | 21,532,912 | 7,060 |
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