Product Details

SNP ID
rs2296924
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:60981792 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CGACTTAGTCATGGGGGGAGGGAAA[A/G]TAATAAACATTTTAATACAGAAATT
Phenotype
MIM: 616518 MIM: 611023
Polymorphism
A/G, 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 75 Intron NP_001166173.1
NM_153811.2 75 Intron NP_722518.2
XM_006720049.3 75 Intron XP_006720112.1
XM_006720050.1 75 Intron XP_006720113.1
XM_011536469.2 75 Intron XP_011534771.1
XM_017021020.1 75 Intron XP_016876509.1
XM_017021021.1 75 Intron XP_016876510.1
XM_017021022.1 75 Intron XP_016876511.1
XM_017021023.1 75 Intron XP_016876512.1
XM_017021024.1 75 Intron XP_016876513.1
XM_017021025.1 75 Intron XP_016876514.1
XM_017021026.1 75 UTR 5 XP_016876515.1
XM_017021027.1 75 Intron XP_016876516.1
XM_017021028.1 75 Intron XP_016876517.1
Gene
TRMT5
Gene Name
tRNA methyltransferase 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020810.3 75 Intron NP_065861.3
XM_005267916.3 75 Intron XP_005267973.2
XM_011537017.2 75 Intron XP_011535319.1

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