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- SNP ID:
- rs200595461
- Gene
-
IFNA8 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.9: 21409455 - 21409455 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
AGCAGACCTTCAACCTCTTCAGCAC[A/G]AAGGACTCATCTGCTGCTTTGGATG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147568
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Literature Links: |
IFNA8 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 |
| IFNA8 - interferon alpha 8 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_002170.3 | 309 | Silent Mutation | ACA,ACG | T,T 93 | NP_002161.2 | |
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