Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAATGGCACCATTCCGTTTACCAGC[C/T]GCACCTTCATTTCTTGAAGGCTGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600004 | ||||||||||||||||||||
Literature Links: |
EPHA5 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 |
EPHA5 - EPH receptor A5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281765.2 | 3627 | Missense Mutation | CAG,CGG | Q,R 1030 | NP_001268694.1 | |
NM_001281766.2 | 3627 | Missense Mutation | CAG,CGG | Q,R 1008 | NP_001268695.1 | |
NM_001281767.2 | 3627 | Intron | NP_001268696.1 | |||
NM_001318761.1 | 3627 | Missense Mutation | CAG,CGG | Q,R 961 | NP_001305690.1 | |
NM_004439.7 | 3627 | Missense Mutation | CAG,CGG | Q,R 1029 | NP_004430.4 | |
NM_182472.4 | 3627 | Missense Mutation | CAG,CGG | Q,R 1007 | NP_872272.2 | |
XM_005265653.3 | 3627 | Missense Mutation | CAG,CGG | Q,R 866 | XP_005265710.1 | |
XM_011531735.2 | 3627 | Missense Mutation | CAG,CGG | Q,R 918 | XP_011530037.1 | |
XM_017007878.1 | 3627 | Missense Mutation | CAG,CGG | Q,R 896 | XP_016863367.1 | |
XM_017007879.1 | 3627 | Intron | XP_016863368.1 | |||
XM_017007880.1 | 3627 | Missense Mutation | CAG,CGG | Q,R 844 | XP_016863369.1 | |
XM_017007881.1 | 3627 | Intron | XP_016863370.1 |