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ATAGCAGTCTATTAATCCCTGAAGA[C/T]AGACCCTGGAACGGCTGCAACCCAA
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SAA2 - serum amyloid A2 | ||||||
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There are no transcripts associated with this gene. |
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 | 555 | Missense Mutation | TAT,TGT | Y,C 160 | NP_001186673.1 |
SAA4 - serum amyloid A4, constitutive | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006512.3 | 555 | Missense Mutation | TAT,TGT | Y,C 82 | NP_006503.2 |