Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGAGCGTGGCCCAGGAGCCTGGGC[C/T]ACCCTGCGGCCTGGGGCTGGGGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 163729 | ||||||||||||||||||||
Literature Links: |
NOS3 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 |
NOS3 - nitric oxide synthase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000603.4 | 91 | Missense Mutation | CCA,CTA | P,L 13 | NP_000594.2 | |
NM_001160109.1 | 91 | Missense Mutation | CCA,CTA | P,L 13 | NP_001153581.1 | |
NM_001160110.1 | 91 | Missense Mutation | CCA,CTA | P,L 13 | NP_001153582.1 | |
NM_001160111.1 | 91 | Missense Mutation | CCA,CTA | P,L 13 | NP_001153583.1 | |
XM_006716002.3 | 91 | Missense Mutation | CCA,CTA | P,L 13 | XP_006716065.1 | |
XM_017012232.1 | 91 | Missense Mutation | CCA,CTA | P,L 13 | XP_016867721.1 | |
XM_017012233.1 | 91 | Intron | XP_016867722.1 | |||
XM_017012234.1 | 91 | Missense Mutation | CCA,CTA | P,L 13 | XP_016867723.1 |