Product Details

SNP ID
rs185538945
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:163069462 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTGCCGCATTTCTTTCCTGCTTG[A/C]GAATTCCAAGCTGTTAAATAAGATG
Phenotype
MIM: 602516
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
RGS4 PubMed Links

Gene Details

Gene
RGS4
Gene Name
regulator of G-protein signaling 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001102445.2 598 Missense Mutation GAG,GCG E90A NP_001095915.1
NM_001113380.1 598 Intron NP_001106851.1
NM_001113381.1 598 UTR 5 NP_001106852.1
NM_005613.5 598 UTR 5 NP_005604.1

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