Product Details

SNP ID

rs200327976

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:177386096 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAGGTCCTGGAGCGCCATGAACC[A/T]CTGCCTGCCAAGCTGGCCCTGGAGG

Phenotype

MIM: 182309

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

SLC34A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs61753440] are located under a probe 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

SLC34A1

Gene Name

solute carrier family 34 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001167579.1	266	Silent Mutation	CCA,CCT	P73P	NP_001161051.1
NM_003052.4	266	Silent Mutation	CCA,CCT	P73P	NP_003043.3
XM_005265975.1	266	Silent Mutation	CCA,CCT	P73P	XP_005266032.1
XM_017009773.1	266	Silent Mutation	CCA,CCT	P73P	XP_016865262.1
XM_017009774.1	266	Intron			XP_016865263.1
XM_017009775.1	266	Silent Mutation	CCA,CCT	P73P	XP_016865264.1

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