Product Details

SNP ID

rs148529934

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:101453040 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGTTCTGCTAGGTCTTCTGTATTC[C/T]GAGATTTTTCTTCAAGGAGTTCATA

Phenotype

MIM: 603652

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TRPC6 PubMed Links

Additional Information

For this assay, SNP(s) [rs12805398] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

TRPC6

Gene Name

transient receptor potential cation channel subfamily C member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004621.5	2638	Missense Mutation	CAG,CGG	Q904R	NP_004612.2
XM_011542968.2	2638	Missense Mutation	CAG,CGG	Q849R	XP_011541270.1
XM_017018221.1	2638	Missense Mutation	CAG,CGG	Q788R	XP_016873710.1
XM_017018222.1	2638	Missense Mutation	CAG,CGG	Q818R	XP_016873711.1

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