Product Details

SNP ID
rs17269265
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:107990031 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATAACCTTGGTCAATATCATAATTC[A/G]TTTAAAATCTGAACCATACTACCTA
Phenotype
MIM: 608761
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC5A7 PubMed Links

Gene Details

Gene
SLC5A7
Gene Name
solute carrier family 5 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305005.2 1669 Intron NP_001291934.1
NM_001305006.2 1669 Intron NP_001291935.1
NM_001305007.2 1669 Intron NP_001291936.1
NM_021815.4 1669 Intron NP_068587.1
XM_011511580.2 1669 Intron XP_011509882.1
XM_017004628.1 1669 Intron XP_016860117.1
XM_017004629.1 1669 UTR 5 XP_016860118.1

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