Product Details

SNP ID
rs144786192
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:58671154 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGGGTGAGCAGGAACCAGACCAG[C/T]GTCTGCAGCACTCGCCGCCGCCGCT
Phenotype
MIM: 614236
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC38A7 PubMed Links

Gene Details

Gene
SLC38A7
Gene Name
solute carrier family 38 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308384.1 1522 Intron NP_001295313.1
NM_018231.2 1522 Silent Mutation ACA,ACG T374T NP_060701.1
XM_017023393.1 1522 Silent Mutation ACA,ACG T374T XP_016878882.1
XM_017023394.1 1522 Intron XP_016878883.1
XM_017023395.1 1522 Intron XP_016878884.1
XM_017023396.1 1522 Intron XP_016878885.1
XM_017023397.1 1522 Intron XP_016878886.1
XM_017023398.1 1522 Intron XP_016878887.1
XM_017023399.1 1522 Intron XP_016878888.1

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