Product Details

SNP ID

rs150018731

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:99978066 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCAGAATTTAAACAGAACCCCAA[A/G]AATTGTCATCTGTATAAAAAAAAGT

Phenotype

MIM: 615650

Polymorphism

A/G, Transition 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	3758	Missense Mutation			NP_001273621.1
NM_001286693.1	3758	Missense Mutation			NP_001273622.1
NM_015668.4	3758	Missense Mutation			NP_056483.3
XM_005250856.2	3758	Missense Mutation			XP_005250913.1
XM_005250857.2	3758	Intron			XP_005250914.1
XM_005250858.2	3758	Missense Mutation			XP_005250915.1
XM_005250860.2	3758	Intron			XP_005250917.1
XM_006716540.2	3758	Missense Mutation			XP_006716603.1
XM_011516957.1	3758	Missense Mutation			XP_011515259.1
XM_011516958.1	3758	Missense Mutation			XP_011515260.1
XM_011516959.2	3758	Intron			XP_011515261.1
XM_017013309.1	3758	Intron			XP_016868798.1
XM_017013310.1	3758	Missense Mutation			XP_016868799.1
XM_017013311.1	3758	Missense Mutation			XP_016868800.1

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