Product Details

SNP ID

rs150365137

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:19055676 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCAGATCCATAATATTAGGAACC[A/G]CTGAATGCCAAAGGGCAGGCCGCAG

Phenotype

MIM: 607228

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MRGPRX2 PubMed Links

Gene Details

Gene

MRGPRX2

Gene Name

MAS related GPR family member X2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303615.1	815	Missense Mutation	CGG,TGG	R243W	NP_001290544.1
NM_054030.3	815	Missense Mutation	CGG,TGG	R243W	NP_473371.1

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