Product Details

SNP ID

rs200140846

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:45253281 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGTGGAGACTGGCACAGTGAACCC[A/G]GGGCTGGAGCTCATGGTAATCACCA

Phenotype

MIM: 606208

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

LOC101928414 PubMed Links

Additional Information

For this assay, SNP(s) [rs11854484] are located under a probe and SNP(s) [rs17215668] 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

LOC101928414

Gene Name

uncharacterized LOC101928414

There are no transcripts associated with this gene.

Gene

SLC28A2

Gene Name

solute carrier family 28 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004212.3	102	Silent Mutation	CCA,CCG	P22P	NP_004203.2
XM_011522198.2	102	Silent Mutation	CCA,CCG	P22P	XP_011520500.1
XM_011522199.1	102	Silent Mutation	CCA,CCG	P22P	XP_011520501.1
XM_011522200.2	102	Silent Mutation	CCA,CCG	P22P	XP_011520502.1
XM_011522201.2	102	Silent Mutation	CCA,CCG	P22P	XP_011520503.1
XM_011522202.2	102	Intron			XP_011520504.1

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