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AGTCTAAGGAATAAAGAGGTGAAGG[A/G]GGCCTGGCATAAACTATTAGAGAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608497 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
OR2F1 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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OR2F1 - olfactory receptor family 2 subfamily F member 1 (gene/pseudogene) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012369.2 | 896 | Intron | NP_036501.2 | |||
XM_011516019.2 | 896 | Intron | XP_011514321.1 | |||
XM_011516020.2 | 896 | Intron | XP_011514322.1 |
OR2F2 - olfactory receptor family 2 subfamily F member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004685.1 | 896 | Missense Mutation | GAG,GGG | E,G 299 | NP_001004685.1 |