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See other RGS3 GT Assays ›
SNP ID:
rs201071186
Gene
RGS3
Gene Name
Set Membership:
-
Chromosome Location:
Chr.9: 113462068 - 113462068 on Build GRCh38
Polymorphism:
G/T, Transversion substitution
Context Sequence [VIC/FAM]:

GTGTCCTCTCTACATCCTGTGGCTT[G/T]AGCCTGAGCTTGCCCATATTCCCTG

Assay ID C_192065675_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 602189

Literature Links:

 RGS3 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
RGS3 - regulator of G-protein signaling 3
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001276260.1 339 Intron NP_001263189.1
NM_001276261.1 339 Intron NP_001263190.1
NM_001276262.1 339 Intron NP_001263191.1
NM_001282922.1 339 Intron NP_001269851.1
NM_001282923.1 339 Intron NP_001269852.1
NM_001322214.1 339 Intron NP_001309143.1
NM_001322215.1 339 Intron NP_001309144.1
NM_017790.4 339 Intron NP_060260.3
NM_130795.3 339 Intron NP_570613.2
NM_134427.2 339 Intron NP_602299.1
NM_144488.5 339 Missense Mutation TTG,TTT L,F 94 NP_652759.3
NM_144489.3 339 Intron NP_652760.2
XM_006717219.2 339 UTR 5 XP_006717282.1
XM_006717220.1 339 Intron XP_006717283.1
XM_006717222.1 339 Intron XP_006717285.1
XM_006717225.1 339 Intron XP_006717288.1
XM_006717226.2 339 Intron XP_006717289.1
XM_006717230.3 339 Intron XP_006717293.1
XM_011518893.1 339 Missense Mutation TTG,TTT L,F 94 XP_011517195.1
XM_011518894.1 339 Intron XP_011517196.1
XM_011518896.1 339 Intron XP_011517198.1
XM_011518897.2 339 Intron XP_011517199.1
XM_011518898.1 339 Intron XP_011517200.1
XM_011518900.1 339 Intron XP_011517202.1
XM_011518901.1 339 Intron XP_011517203.1
XM_017015003.1 339 Missense Mutation TTG,TTT L,F 94 XP_016870492.1
XM_017015004.1 339 Intron XP_016870493.1
XM_017015005.1 339 Intron XP_016870494.1
XM_017015006.1 339 Intron XP_016870495.1

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