Product Details

SNP ID

rs200191596

Assay Type

Functionally Tested

NCBI dbSNP Submissions

6

Location

Chr.1:225777976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCAGACCTGGGAGGAGTTCAGCCG[C/T]GCTGCCGAGAAGCTTTACCTCGCTG

Phenotype

MIM: 600707

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SRP9 PubMed Links

Additional Information

For this assay, SNP(s) [rs1461957] 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

SRP9

Gene Name

signal recognition particle 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130440.1		Intron			NP_001123912.1
NM_003133.5		Intron			NP_003124.1

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