Product Details

SNP ID

rs114747263

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:33099404 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGCGTGTTCATTGCCTGGTACATC[C/T]GGTATGCAATCTTCTGGCTTAGTCT

Phenotype

MIM: 607331

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RP9 PubMed Links

Additional Information

For this assay, SNP(s) [rs17472556] are located under a primer 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

RP9

Gene Name

retinitis pigmentosa 9 (autosomal dominant)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203288.1	710	Intron			NP_976033.1
XM_011515468.2	710	Silent Mutation	CCA,CCG	P38P	XP_011513770.1

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