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AATGCAACACTGCCACATGTGCAAC[A/G]CAGCGCCTGGCAAATTTTTTAGTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147940 MIM: 602883 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IAPP 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
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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IAPP - islet amyloid polypeptide | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000415.2 | 227 | Silent Mutation | ACA,ACG | T,T 42 | NP_000406.1 | |
XM_017019253.1 | 227 | Silent Mutation | ACA,ACG | T,T 42 | XP_016874742.1 |
SLCO1A2 - solute carrier organic anion transporter family member 1A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021094.3 | 227 | Intron | NP_066580.1 | |||
NM_134431.3 | 227 | Intron | NP_602307.1 | |||
XM_005253474.3 | 227 | Intron | XP_005253531.1 | |||
XM_005253477.3 | 227 | Intron | XP_005253534.1 | |||
XM_011520818.1 | 227 | Intron | XP_011519120.1 | |||
XM_011520819.1 | 227 | Intron | XP_011519121.1 | |||
XM_011520820.2 | 227 | Intron | XP_011519122.1 | |||
XM_011520821.2 | 227 | Intron | XP_011519123.1 | |||
XM_017019849.1 | 227 | Intron | XP_016875338.1 | |||
XM_017019850.1 | 227 | Intron | XP_016875339.1 |