Product Details

SNP ID
rs1013940
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:107992192 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGGCCTAGCTTGGGCTCAGGCACCA[A/G]TTGGATATTCTCTTAGTCTGATTTT
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_001305005.2 566 Missense Mutation ATT,GTT I89V NP_001291934.1
NM_001305006.2 566 UTR 5 NP_001291935.1
NM_001305007.2 566 UTR 5 NP_001291936.1
NM_021815.4 566 Missense Mutation ATT,GTT I89V NP_068587.1
XM_011511580.2 566 Intron XP_011509882.1
XM_017004628.1 566 Intron XP_016860117.1
XM_017004629.1 566 UTR 5 XP_016860118.1

View Full Product Details