Product Details

SNP ID

rs16933949

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:113462172 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTCAAACTTCTCCAGCCAGGAAGA[A/G]GATCACGCATGCCAAAGTCCAGGGT

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	443	Intron			NP_001263189.1
NM_001276261.1	443	Intron			NP_001263190.1
NM_001276262.1	443	Intron			NP_001263191.1
NM_001282922.1	443	Intron			NP_001269851.1
NM_001282923.1	443	Intron			NP_001269852.1
NM_001322214.1	443	Intron			NP_001309143.1
NM_001322215.1	443	Intron			NP_001309144.1
NM_017790.4	443	Intron			NP_060260.3
NM_130795.3	443	Intron			NP_570613.2
NM_134427.2	443	Intron			NP_602299.1
NM_144488.5	443	Missense Mutation	AAG,AGG	K129R	NP_652759.3
NM_144489.3	443	Intron			NP_652760.2
XM_006717219.2	443	Missense Mutation	AAG,AGG	K25R	XP_006717282.1
XM_006717220.1	443	Intron			XP_006717283.1
XM_006717222.1	443	Intron			XP_006717285.1
XM_006717225.1	443	Intron			XP_006717288.1
XM_006717226.2	443	Intron			XP_006717289.1
XM_006717230.3	443	Intron			XP_006717293.1
XM_011518893.1	443	Missense Mutation	AAG,AGG	K129R	XP_011517195.1
XM_011518894.1	443	Intron			XP_011517196.1
XM_011518896.1	443	Intron			XP_011517198.1
XM_011518897.2	443	Intron			XP_011517199.1
XM_011518898.1	443	Intron			XP_011517200.1
XM_011518900.1	443	Intron			XP_011517202.1
XM_011518901.1	443	Intron			XP_011517203.1
XM_017015003.1	443	Missense Mutation	AAG,AGG	K129R	XP_016870492.1
XM_017015004.1	443	Intron			XP_016870493.1
XM_017015005.1	443	Intron			XP_016870494.1
XM_017015006.1	443	Intron			XP_016870495.1

View Full Product Details