Search Thermo Fisher Scientific
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AGATGGGGATCCCCACAGTGTTCAC[C/G]TGGTCCTTGAGTCCCAGCAGGCTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
18 submissions
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Phenotype: |
MIM: 176946 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EPHA2 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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EPHA2 - EPH receptor A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017000534.1 | 2982 | Missense Mutation | CAC,CAG | H,Q 965 | XP_016856023.1 | |
XM_017000535.1 | 2982 | Missense Mutation | CAC,CAG | H,Q 957 | XP_016856024.1 | |
XM_017000536.1 | 2982 | Missense Mutation | CAC,CAG | H,Q 914 | XP_016856025.1 | |
XM_017000537.1 | 2982 | Intron | XP_016856026.1 |