Product Details

SNP ID

rs12509294

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:103026309 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGCTTAAACATTACATATTTCAATA[C/T]GCATCTTGAAAAAAGTAGCAGCTTT

Phenotype

MIM: 611527 MIM: 611789

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC9B1 PubMed Links

Additional Information

For this assay, SNP(s) [rs111508094] 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

SLC9B1

Gene Name

solute carrier family 9 member B1

There are no transcripts associated with this gene.

Gene

SLC9B2

Gene Name

solute carrier family 9 member B2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300754.1	1770	UTR 3			NP_001287683.1
NM_001300756.1	1770	UTR 3			NP_001287685.1
NM_178833.5	1770	UTR 3			NP_849155.2
XM_006714085.2	1770	Intron			XP_006714148.1
XM_006714086.3	1770	UTR 3			XP_006714149.1

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