Product Details

SNP ID

rs145265988

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:46775561 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGACCGTGGCATCCCCTGCGGGCCC[C/T]CGATAGTGTTTGAGGAGGGGGTTTC

Phenotype

MIM: 109190

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC1A5 PubMed Links

Additional Information

For this assay, SNP(s) [rs3027961] 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

SLC1A5

Gene Name

solute carrier family 1 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145144.1	1249	Silent Mutation	CGA,CGG	R297R	NP_001138616.1
NM_001145145.1	1249	Silent Mutation	CGA,CGG	R323R	NP_001138617.1
NM_005628.2	1249	Silent Mutation	CGA,CGG	R525R	NP_005619.1
XM_005259167.4	1249	Intron			XP_005259224.1

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