Product Details

SNP ID

rs141434863

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:113461831 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGTCTCCCCTTTGGGAGGAGGCTC[C/T]ACAGTGGTCCCTGGCGAAGTTGTGA

Phenotype

MIM: 602189

Polymorphism

C/T, 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	416	Intron			NP_001263189.1
NM_001276261.1	416	Intron			NP_001263190.1
NM_001276262.1	416	Intron			NP_001263191.1
NM_001282922.1	416	Intron			NP_001269851.1
NM_001282923.1	416	Intron			NP_001269852.1
NM_001322214.1	416	Intron			NP_001309143.1
NM_001322215.1	416	Intron			NP_001309144.1
NM_017790.4	416	Intron			NP_060260.3
NM_130795.3	416	Intron			NP_570613.2
NM_134427.2	416	Intron			NP_602299.1
NM_144488.5	416	Missense Mutation	CAC,TAC	H69Y	NP_652759.3
NM_144489.3	416	Intron			NP_652760.2
XM_006717219.2	416	Intron			XP_006717282.1
XM_006717220.1	416	Intron			XP_006717283.1
XM_006717222.1	416	Intron			XP_006717285.1
XM_006717225.1	416	Intron			XP_006717288.1
XM_006717226.2	416	Intron			XP_006717289.1
XM_006717230.3	416	Intron			XP_006717293.1
XM_011518893.1	416	Missense Mutation	CAC,TAC	H69Y	XP_011517195.1
XM_011518894.1	416	Intron			XP_011517196.1
XM_011518896.1	416	Intron			XP_011517198.1
XM_011518897.2	416	Intron			XP_011517199.1
XM_011518898.1	416	Intron			XP_011517200.1
XM_011518900.1	416	Intron			XP_011517202.1
XM_011518901.1	416	Intron			XP_011517203.1
XM_017015003.1	416	Missense Mutation	CAC,TAC	H69Y	XP_016870492.1
XM_017015004.1	416	Intron			XP_016870493.1
XM_017015005.1	416	Intron			XP_016870494.1
XM_017015006.1	416	Intron			XP_016870495.1

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