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AGCTGGCATCTGTGGCCTGGGTTAT[A/G]AGTCTGGTTCAATCGATAGTCCAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
OR2H1 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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OR2H1 - olfactory receptor family 2 subfamily H member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318014.1 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | NP_001304943.1 | |
NM_001318022.1 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | NP_001304951.1 | |
NM_030883.4 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | NP_112145.1 | |
XM_011514470.2 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_011512772.1 | |
XM_011514472.2 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_011512774.1 | |
XM_011514473.2 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_011512775.1 | |
XM_011514479.2 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_011512781.1 | |
XM_011514483.2 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_011512785.1 | |
XM_011514484.2 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_011512786.1 | |
XM_017010737.1 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_016866226.1 | |
XM_017010738.1 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_016866227.1 | |
XM_017010739.1 | 2189 | Missense Mutation | ATA,ATG | I,M 149 | XP_016866228.1 | |
XM_017010740.1 | 2189 | Missense Mutation | ATA,ATG | I,M 71 | XP_016866229.1 |
OR5V1 - olfactory receptor family 5 subfamily V member 1 | ||||||
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There are no transcripts associated with this gene. |