Product Details
- SNP ID
-
rs141329281
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:1225503 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATGGCTCATGCCCCAGAACCGGACC[C/T]GGCCGCCTGCGACCTCGGGGATGAG
- Phenotype
-
MIM: 610300
MIM: 608893
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SLC6A18
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs7704058] are located under a probe 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
- SLC6A18
- Gene Name
- solute carrier family 6 member 18
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_182632.2 |
149 |
Missense Mutation |
CCG,CTG |
P9L |
NP_872438.2 |
- Gene
- SLC6A19
- Gene Name
- solute carrier family 6 member 19
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