Product Details

SNP ID
rs138461251
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:25662564 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCGATAAGTACCTCGAAGGGGCC[A/G]CAGGTCAGCAGCCCACTGCCCCTGA
Phenotype
MIM: 604217
Polymorphism
A/G, Transition 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_001177998.1 168 Missense Mutation ACA,GCA T22A NP_001171469.1
NM_001177999.1 168 Missense Mutation ACA,GCA T22A NP_001171470.1
NM_006424.2 168 Missense Mutation ACA,GCA T22A NP_006415.2

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