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CCGGAGGAAGGCCATCTTGGCGCTG[C/T]TCAGTGTCTGGGTCTTGTCCACCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 104220 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADRA1B 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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ADRA1B - adrenoceptor alpha 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000679.3 | 672 | Missense Mutation | CTC,TTC | L,F 167 | NP_000670.1 | |
XM_005265818.3 | 672 | Missense Mutation | CTC,TTC | L,F 167 | XP_005265875.1 | |
XM_005265819.2 | 672 | Missense Mutation | CTC,TTC | L,F 167 | XP_005265876.1 | |
XM_006714821.3 | 672 | Missense Mutation | CTC,TTC | L,F 167 | XP_006714884.1 | |
XM_011534435.1 | 672 | Missense Mutation | CTC,TTC | L,F 167 | XP_011532737.1 | |
XM_011534437.2 | 672 | Missense Mutation | CTC,TTC | L,F 167 | XP_011532739.1 | |
XM_011534438.2 | 672 | Missense Mutation | CTC,TTC | L,F 167 | XP_011532740.1 |