Product Details

SNP ID
rs200454912
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:177386233 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCCCCCATCCAGAGTCCAGGCTGG[G/T]CCCCAAGCTGCGCCAGGCTGGCGCC
Phenotype
MIM: 182309
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SLC34A1 PubMed Links

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_001167579.1 319 Missense Mutation GGC,GTC G91V NP_001161051.1
NM_003052.4 319 Missense Mutation GGC,GTC G91V NP_003043.3
XM_005265975.1 319 Missense Mutation GGC,GTC G91V XP_005266032.1
XM_017009773.1 319 Missense Mutation GGC,GTC G91V XP_016865262.1
XM_017009774.1 319 Intron XP_016865263.1
XM_017009775.1 319 Missense Mutation GGC,GTC G91V XP_016865264.1

View Full Product Details