Product Details

SNP ID
rs149915773
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:93566862 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCGCGGTGGAGACAACCGTGCTG[A/G]TGCTCATCTTTGCAGTGTCGCTGCT
Phenotype
MIM: 609044
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FFAR4 PubMed Links

Gene Details

Gene
FFAR4
Gene Name
free fatty acid receptor 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195755.1 684 Missense Mutation ATG,GTG M48V NP_001182684.1
NM_181745.3 684 Missense Mutation ATG,GTG M48V NP_859529.2
XM_011539746.2 684 Missense Mutation ATG,GTG M48V XP_011538048.1

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