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AGGAAGCTCAGTATTTCTCAGGCAG[A/G]CCAGCAGGTCGGAAGTGATTGGGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 104751 MIM: 104752 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SAA2 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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SAA2 - serum amyloid A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127380.2 | 427 | Intron | NP_001120852.1 | |||
NM_030754.4 | 427 | Silent Mutation | GGC,GGT | G,G 117 | NP_110381.2 |
SAA2-SAA4 - SAA2-SAA4 readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199744.1 | 427 | Intron | NP_001186673.1 |
SAA4 - serum amyloid A4, constitutive | ||||||
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There are no transcripts associated with this gene. |