Product Details

SNP ID
rs112465391
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:177368162 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATCGCTCCCTCTTCACTAGAGCTG[A/G]GCGGGACTGCAAACGCCGCCTTGCG
Phenotype
MIM: 602513
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RGS14 PubMed Links

Gene Details

Gene
RGS14
Gene Name
regulator of G-protein signaling 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006480.4 1094 Missense Mutation AGC,GGC S249G NP_006471.2
XM_005265794.4 1094 Missense Mutation AGC,GGC S249G XP_005265851.1
XM_005265795.4 1094 Missense Mutation AGC,GGC S249G XP_005265852.1

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