Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCACCTCGCTGGCCAGCTGCTGCC[A/G]CAGGATGTCCTGAACATAGACCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 163730 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NOS2 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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NOS2 - nitric oxide synthase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000625.4 | 3042 | Missense Mutation | CGG,TGG | R,W 1061 | NP_000616.3 | |
XM_011524859.2 | 3042 | Missense Mutation | CGG,TGG | R,W 1061 | XP_011523161.1 | |
XM_011524860.2 | 3042 | Missense Mutation | CGG,TGG | R,W 1060 | XP_011523162.1 | |
XM_011524861.1 | 3042 | Missense Mutation | CGG,TGG | R,W 1037 | XP_011523163.1 | |
XM_011524862.1 | 3042 | Missense Mutation | CGG,TGG | R,W 839 | XP_011523164.1 |