Product Details

SNP ID

rs144794319

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:27100329 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTTACTGCCCCTTGGGGAAGAAC[A/G]GTTCTCCCTCCCCAGGCTCAGGGTG

Phenotype

MIM: 107310

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC9A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs4266911] 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

SLC9A1

Gene Name

solute carrier family 9 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003047.4	2300	Missense Mutation	CCG,CTG	P809L	NP_003038.2
XM_011542021.2	2300	Missense Mutation	CCG,CTG	P699L	XP_011540323.1

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