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CCCAATTGTATATCTGATAATATTT[G/T]TCTGGGGAGTCTTGGGAAATGGGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605666 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYSLTR2 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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CYSLTR2 - cysteinyl leukotriene receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308465.1 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_001295394.1 | |
NM_001308467.1 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_001295396.1 | |
NM_001308468.1 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_001295397.1 | |
NM_001308469.1 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_001295398.1 | |
NM_001308470.1 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_001295399.1 | |
NM_001308471.1 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_001295400.1 | |
NM_001308476.1 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_001295405.1 | |
NM_020377.3 | 849 | Missense Mutation | GTC,TTC | V,F 50 | NP_065110.1 |