Product Details

SNP ID

rs150066286

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:132417702 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTCTCCAGCCGCTGGACCGTGTT[C/G]CAGTCCAGCATCTTCGGCGCCTTCG

Phenotype

MIM: 602886

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

GPR39 PubMed Links

Gene Details

Gene

GPR39

Gene Name

G protein-coupled receptor 39

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001508.2	1129	Missense Mutation	TTC,TTG	F220L	NP_001499.1
XM_011511021.2	1129	Missense Mutation	TTC,TTG	F220L	XP_011509323.1

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