Product Details

SNP ID
rs4869676
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:36609059 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACTGGTGCTGACTTGAAGCTGAGT[A/T]TCAACGCTTAGGCACAGAGACCGAA
Phenotype
MIM: 600111
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
SLC1A3 PubMed Links

Gene Details

Gene
SLC1A3
Gene Name
solute carrier family 1 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166695.2 1112 Intron NP_001160167.1
NM_001166696.2 1112 UTR 3 NP_001160168.1
NM_001289939.1 1112 Intron NP_001276868.1
NM_001289940.1 1112 Intron NP_001276869.1
NM_004172.4 1112 Intron NP_004163.3
XM_005248342.2 1112 Intron XP_005248399.1
XM_011514084.2 1112 Intron XP_011512386.1

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