Product Details

SNP ID

rs141141857

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:19055691 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTAGGAACCACTGAATGCCAAAGG[C/G]CAGGCCGCAGAGGAGGAACACCAGC

Phenotype

MIM: 607228

Polymorphism

C/G, Transversion 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	800	Missense Mutation	CCC,GCC	P238A	NP_001290544.1
NM_054030.3	800	Missense Mutation	CCC,GCC	P238A	NP_473371.1

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