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GCAGCCATCTTGGCACAGAGTGTGG[A/T]GGTCATAATTATAGGGTAGTGGAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
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Literature Links: |
OR6N1 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 |
OR6N1 - olfactory receptor family 6 subfamily N member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005185.1 | 412 | Intron | NP_001005185.1 | |||
XM_017000325.1 | 412 | Intron | XP_016855814.1 | |||
XM_017000326.1 | 412 | Intron | XP_016855815.1 | |||
XM_017000327.1 | 412 | Intron | XP_016855816.1 |
OR6N2 - olfactory receptor family 6 subfamily N member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005278.1 | 412 | Missense Mutation | ACC,TCC | T,S 138 | NP_001005278.1 |