Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCTCTAATCAGTCTCGGAAGTTCA[A/C]GATCCTGTTTTTCAAAAAATAAGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
OR1E2 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 |
OR1E2 - olfactory receptor family 1 subfamily E member 2 | ||||||
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There are no transcripts associated with this gene. |
SPATA22 - spermatogenesis associated 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170695.1 | 1143 | Missense Mutation | NP_001164166.1 | |||
NM_001170696.1 | 1143 | Missense Mutation | NP_001164167.1 | |||
NM_001170697.1 | 1143 | Missense Mutation | NP_001164168.1 | |||
NM_001170698.1 | 1143 | Missense Mutation | NP_001164169.1 | |||
NM_001170699.1 | 1143 | Silent Mutation | NP_001164170.1 | |||
NM_001321336.1 | 1143 | Missense Mutation | NP_001308265.1 | |||
NM_001321337.1 | 1143 | Missense Mutation | NP_001308266.1 | |||
NM_032598.4 | 1143 | Missense Mutation | NP_115987.2 |