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AACCCAGGGAATATCACAGGTGCCC[A/G]GGGACTCACGGGCACCCTTCGGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 109135 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AXL 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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AXL - AXL receptor tyrosine kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278599.1 | 337 | Intron | NP_001265528.1 | |||
NM_001699.5 | 337 | Missense Mutation | CAG,CGG | Q,R 48 | NP_001690.2 | |
NM_021913.4 | 337 | Missense Mutation | CAG,CGG | Q,R 48 | NP_068713.2 |