Product Details

SNP ID
rs78717434
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:60991538 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAGGAGCCAGGATTCAAACCCACA[C/T]AGTCTGGCTCTAAAATTGTGCTCAC
Phenotype
MIM: 616518
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC38A6 PubMed Links

Gene Details

Gene
SLC38A6
Gene Name
solute carrier family 38 member 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001172702.1 Intron NP_001166173.1
NM_153811.2 Intron NP_722518.2
XM_006720049.3 Intron XP_006720112.1
XM_006720050.1 Intron XP_006720113.1
XM_011536469.2 Intron XP_011534771.1
XM_017021020.1 Intron XP_016876509.1
XM_017021021.1 Intron XP_016876510.1
XM_017021022.1 Intron XP_016876511.1
XM_017021023.1 Intron XP_016876512.1
XM_017021024.1 Intron XP_016876513.1
XM_017021025.1 Intron XP_016876514.1
XM_017021026.1 Intron XP_016876515.1
XM_017021027.1 Intron XP_016876516.1
XM_017021028.1 Intron XP_016876517.1

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