Product Details

SNP ID
rs268818
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:57564874 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATCTCCATCACTTCAAAATAAAAG[C/T]CCATACCCATTAACTCCTCAGCTTC
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC35F4 PubMed Links

Gene Details

Gene
SLC35F4
Gene Name
solute carrier family 35 member F4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206920.1 Intron NP_001193849.1
NM_001306087.1 Intron NP_001293016.1
XM_011536720.2 Intron XP_011535022.1
XM_011536721.2 Intron XP_011535023.1
XM_011536723.2 Intron XP_011535025.1
XM_011536724.2 Intron XP_011535026.1
XM_011536725.1 Intron XP_011535027.1
XM_017021258.1 Intron XP_016876747.1
XM_017021259.1 Intron XP_016876748.1
XM_017021260.1 Intron XP_016876749.1
XM_017021261.1 Intron XP_016876750.1

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