Product Details

SNP ID

rs3729977

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:116172971 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCTTTAATATTCATAGCAACATGC[C/T]ATTTTGGAATTAGAAAACACTTACT

Phenotype

MIM: 300034

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

AGTR2 PubMed Links

Gene Details

Gene

AGTR2

Gene Name

angiotensin II receptor type 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000686.4	796	Missense Mutation	CAT,TAT	H231Y	NP_000677.2
XM_011537533.1	796	Missense Mutation	CAT,TAT	H231Y	XP_011535835.1

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