Product Details

SNP ID
rs192936403
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:42546483 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTCTTACAGCCCCATGGCTGGGG[G/T]TTATGGAGTGATGGGTGACGATGGT
Phenotype
MIM: 158378
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC20A2 PubMed Links

Gene Details

Gene
SLC20A2
Gene Name
solute carrier family 20 member 2
There are no transcripts associated with this gene.

Gene
SMIM19
Gene Name
small integral membrane protein 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135674.1 767 Missense Mutation GGT,GTT G4V NP_001129146.1
NM_001135675.1 767 Missense Mutation GGT,GTT G4V NP_001129147.1
NM_001135676.1 767 Missense Mutation GGT,GTT G4V NP_001129148.1
NM_138436.3 767 Missense Mutation GGT,GTT G4V NP_612445.2
XM_005273398.4 767 Missense Mutation GGT,GTT G11V XP_005273455.1

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