Product Details

SNP ID
rs141143019
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:113460301 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGGGAGGTTGAGATGGGCAGATC[A/G]CAAGGTCAGGAGATCGAGACCATCC
Phenotype
MIM: 602189
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RGS3 PubMed Links

Gene Details

Gene
RGS3
Gene Name
regulator of G-protein signaling 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001276260.1 256 Intron NP_001263189.1
NM_001276261.1 256 Intron NP_001263190.1
NM_001276262.1 256 Intron NP_001263191.1
NM_001282922.1 256 Intron NP_001269851.1
NM_001282923.1 256 Intron NP_001269852.1
NM_001322214.1 256 Intron NP_001309143.1
NM_001322215.1 256 Intron NP_001309144.1
NM_017790.4 256 Intron NP_060260.3
NM_130795.3 256 Intron NP_570613.2
NM_134427.2 256 Intron NP_602299.1
NM_144488.5 256 Silent Mutation TCA,TCG S15S NP_652759.3
NM_144489.3 256 Intron NP_652760.2
XM_006717219.2 256 UTR 5 XP_006717282.1
XM_006717220.1 256 Intron XP_006717283.1
XM_006717222.1 256 Intron XP_006717285.1
XM_006717225.1 256 Intron XP_006717288.1
XM_006717226.2 256 Intron XP_006717289.1
XM_006717230.3 256 Intron XP_006717293.1
XM_011518893.1 256 Silent Mutation TCA,TCG S15S XP_011517195.1
XM_011518894.1 256 Intron XP_011517196.1
XM_011518896.1 256 Intron XP_011517198.1
XM_011518897.2 256 Intron XP_011517199.1
XM_011518898.1 256 Intron XP_011517200.1
XM_011518900.1 256 Intron XP_011517202.1
XM_011518901.1 256 Intron XP_011517203.1
XM_017015003.1 256 Silent Mutation TCA,TCG S15S XP_016870492.1
XM_017015004.1 256 Intron XP_016870493.1
XM_017015005.1 256 Intron XP_016870494.1
XM_017015006.1 256 Intron XP_016870495.1

View Full Product Details