Product Details

SNP ID: rs140574615
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:26994857 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAAAAGCATCTCCTACGACCTAGAC[A/G]GGGAAGAGAGCTATGGCAAGTACCT
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: FIBIN PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203371.1	777	Missense Mutation	AGG,GGG	R111G	NP_976249.1