Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 139312 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GNAL 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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GNAL - G protein subunit alpha L | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142339.2 | 686 | Intron | NP_001135811.1 | |||
NM_001261443.1 | 686 | Intron | NP_001248372.1 | |||
NM_001261444.1 | 686 | Intron | NP_001248373.1 | |||
NM_182978.3 | 686 | Missense Mutation | AAG,AGG | K,R 46 | NP_892023.1 | |
XM_006722324.2 | 686 | Missense Mutation | AAG,AGG | K,R 46 | XP_006722387.1 |