Product Details

SNP ID
rs4130205
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:99977655 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTATATAAAGCATGTTCTACAAGG[G/T]GGAGGAACGTTATTGCAGCGGATGC
Phenotype
MIM: 615650
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
RGS22 PubMed Links

Gene Details

Gene
RGS22
Gene Name
regulator of G-protein signaling 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286692.1 Intron NP_001273621.1
NM_001286693.1 Intron NP_001273622.1
NM_015668.4 Intron NP_056483.3
XM_005250856.2 Intron XP_005250913.1
XM_005250857.2 Intron XP_005250914.1
XM_005250858.2 Intron XP_005250915.1
XM_005250860.2 Intron XP_005250917.1
XM_006716540.2 Intron XP_006716603.1
XM_011516957.1 Intron XP_011515259.1
XM_011516958.1 Intron XP_011515260.1
XM_011516959.2 Intron XP_011515261.1
XM_017013309.1 Intron XP_016868798.1
XM_017013310.1 Intron XP_016868799.1
XM_017013311.1 Intron XP_016868800.1

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