Product Details

SNP ID
rs149230836
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:128966209 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCACTTCTTGCAGAAACTCCTGTT[C/G]CCTTACTTTTGGGATGACTTCTGGT
Phenotype
MIM: 604196
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC27A6 PubMed Links

Gene Details

Gene
SLC27A6
Gene Name
solute carrier family 27 member 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001017372.2 907 Missense Mutation TTC,TTG F24L NP_001017372.1
NM_001317984.1 907 Missense Mutation TTC,TTG F24L NP_001304913.1
NM_014031.4 907 Missense Mutation TTC,TTG F24L NP_054750.1

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