Product Details

SNP ID: rs409093
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:35450346 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTGTGGATCATGCTCTCCCAGCCCC[A/T]TGTGGGGGCCCAGAGGCGGCGCCGA
Phenotype: MIM: 603823
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: FFAR2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005306.2	632	Missense Mutation	CAT,CTT	H211L	NP_005297.1
XM_017026709.1	632	Missense Mutation	CAT,CTT	H211L	XP_016882198.1
XM_017026710.1	632	Missense Mutation	CAT,CTT	H211L	XP_016882199.1
XM_017026711.1	632	Missense Mutation	CAT,CTT	H211L	XP_016882200.1