Product Details

SNP ID
rs17708892
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:150195223 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCCTCTGCTTCGTGATAAGGAGCT[A/G]TATCTGCCTGCCGATGATCACTGCA
Phenotype
MIM: 606205
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC6A7 PubMed Links

Gene Details

Gene
SLC6A7
Gene Name
solute carrier family 6 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014228.4 773 Intron NP_055043.2
XM_017009767.1 773 Intron XP_016865256.1
XM_017009768.1 773 Intron XP_016865257.1
XM_017009769.1 773 UTR 5 XP_016865258.1
XM_017009770.1 773 Intron XP_016865259.1

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