Product Details

SNP ID
rs994426
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:3302249 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTGTGGCCTCCGTGTGTCCTGTTC[A/G]CTTTTCCTGAAGCCAGGTCATCACC
Phenotype
MIM: 602512
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RGS12 PubMed Links

Gene Details

Gene
RGS12
Gene Name
regulator of G-protein signaling 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002926.3 Intron NP_002917.1
NM_198227.1 Intron NP_937870.1
NM_198229.2 Intron NP_937872.1
XM_006713905.1 Intron XP_006713968.1
XM_006713906.2 Intron XP_006713969.1
XM_006713907.1 Intron XP_006713970.1
XM_011513543.2 Intron XP_011511845.1
XM_017008529.1 Intron XP_016864018.1
XM_017008530.1 Intron XP_016864019.1
XM_017008531.1 Intron XP_016864020.1
XM_017008532.1 Intron XP_016864021.1
XM_017008533.1 Intron XP_016864022.1
XM_017008534.1 Intron XP_016864023.1

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