Product Details
- SNP ID
-
rs201934315
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:119319084 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTTTTGGCTTCTACTCCTTCATAT[A/G]CATAAGTCTGAAAGGTGTTAACAAA
- Phenotype
-
MIM: 134640
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
FABP2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs1511025] are located under a probe and SNP(s) [rs1511024] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- FABP2
- Gene Name
- fatty acid binding protein 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_000134.3 |
415 |
Missense Mutation |
GCA,GTA |
A119V |
NP_000125.2 |
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