Product Details
- SNP ID
-
rs200230812
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:94115942 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTTGTGGCTACTCTGCAGTCACTG[C/G]GTAAGTATCCTGGCGGGGCTTGCTG
- Phenotype
-
MIM: 600009
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
IFI27
PubMed Links
Gene Details
- Gene
- IFI27
- Gene Name
- interferon alpha inducible protein 27
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001130080.2 |
462 |
Missense Mutation |
CGA,GGA |
R95G |
NP_001123552.1 |
| NM_001288952.1 |
462 |
Missense Mutation |
CGA,GGA |
R95G |
NP_001275881.1 |
| NM_001288954.1 |
462 |
Missense Mutation |
CGA,GGA |
R92G |
NP_001275883.1 |
| NM_001288956.1 |
462 |
Missense Mutation |
CGA,GGA |
R95G |
NP_001275885.1 |
| NM_001288957.1 |
462 |
Missense Mutation |
CGA,GGA |
R92G |
NP_001275886.1 |
| NM_001288958.1 |
462 |
Missense Mutation |
CGA,GGA |
R92G |
NP_001275887.1 |
| NM_001288959.1 |
462 |
Missense Mutation |
CGA,GGA |
R52G |
NP_001275888.1 |
| NM_001288960.1 |
462 |
Missense Mutation |
CGA,GGA |
R47G |
NP_001275889.1 |
| NM_001288995.1 |
462 |
Missense Mutation |
CGA,GGA |
R92G |
NP_001275924.1 |
| NM_005532.4 |
462 |
Missense Mutation |
CGA,GGA |
R92G |
NP_005523.3 |
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