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- SNP ID:
- rs79274528
- Gene
-
EPHA8 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 22586538 - 22586538 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GGGACCAGCTGTGTGCCCGCTGCCC[C/T]CCCCACAGCCACTCCGCAGCTCCAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 176945
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Literature Links: |
EPHA8 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 |
| EPHA8 - EPH receptor A8 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| XM_011540969.1 | 1170 | Silent Mutation | CCC,CCT | P,P 219 | XP_011539271.1 | |
| XM_011540970.1 | 1170 | Silent Mutation | CCC,CCT | P,P 219 | XP_011539272.1 | |
| XM_011540972.1 | 1170 | Silent Mutation | CCC,CCT | P,P 219 | XP_011539274.1 | |
| XM_011540973.1 | 1170 | Silent Mutation | CCC,CCT | P,P 219 | XP_011539275.1 | |
| XM_011540975.2 | 1170 | Intron | XP_011539277.1 | |||
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