Product Details

SNP ID

rs148305209

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:25662723 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTTCAGCAGATAACACTGAGGCAC[C/G]TGTAACCAAGATTGAACTTCTGCCG

Phenotype

MIM: 604217

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC34A2 PubMed Links

Gene Details

Gene

SLC34A2

Gene Name

solute carrier family 34 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001177998.1	232	Missense Mutation	CCT,CGT	P43R	NP_001171469.1
NM_001177999.1	232	Missense Mutation	CCT,CGT	P43R	NP_001171470.1
NM_006424.2	232	Missense Mutation	CCT,CGT	P44R	NP_006415.2

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