Product Details

SNP ID
rs269973
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:45198673 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCTCTTACACAGCTTTGTAAGTTA[G/T]GCATTTTATTTCTATTGTTTTAGTG
Phenotype
MIM: 601611
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC14A2 PubMed Links

Gene Details

Gene
SLC14A2
Gene Name
solute carrier family 14 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242692.1 Intron NP_001229621.1
NM_007163.3 Intron NP_009094.3
XM_017026015.1 Intron XP_016881504.1
XM_017026016.1 Intron XP_016881505.1

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