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ACTTGTGGTAGACGTCGATGATAGA[G/T]TTCAAGGCTTTCTCCAGCTCGGTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
|
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Phenotype: |
MIM: 123885 | ||||||||||||||||||||
Literature Links: |
S100A8 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 |
S100A8 - S100 calcium binding protein A8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319196.1 | 172 | Missense Mutation | AAA,AAC | K,N 34 | NP_001306125.1 | |
NM_001319197.1 | 172 | Missense Mutation | AAA,AAC | K,N 33 | NP_001306126.1 | |
NM_001319198.1 | 172 | Missense Mutation | AAA,AAC | K,N 18 | NP_001306127.1 | |
NM_001319201.1 | 172 | Missense Mutation | AAA,AAC | K,N 10 | NP_001306130.1 | |
NM_002964.4 | 172 | Missense Mutation | AAA,AAC | K,N 10 | NP_002955.2 |