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CAATATAGCACATACAATAGGTGTT[C/T]TGGTTTTTTTGAGGCACAGTTTCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 146680 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IDE PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
IDE - insulin degrading enzyme | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001165946.1 | Intron | NP_001159418.1 | ||||
NM_001322793.1 | Intron | NP_001309722.1 | ||||
NM_001322794.1 | Intron | NP_001309723.1 | ||||
NM_001322795.1 | Intron | NP_001309724.1 | ||||
NM_001322796.1 | Intron | NP_001309725.1 | ||||
NM_001322797.1 | Intron | NP_001309726.1 | ||||
NM_004969.3 | Intron | NP_004960.2 | ||||
XM_017016187.1 | Intron | XP_016871676.1 | ||||
XM_017016188.1 | Intron | XP_016871677.1 | ||||
XM_017016189.1 | Intron | XP_016871678.1 | ||||
XM_017016190.1 | Intron | XP_016871679.1 |