Product Details

SNP ID
rs146303356
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:46769286 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTGAAGCCTTTCTGAAACTCACCT[A/G]TGAATCCGAAGATGTATTTTATAGT
Phenotype
MIM: 608065
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SLC38A4 PubMed Links

Gene Details

Gene
SLC38A4
Gene Name
solute carrier family 38 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143824.1 1841 Missense Mutation ACA,ATA T481I NP_001137296.1
NM_018018.4 1841 Missense Mutation ACA,ATA T481I NP_060488.2
XM_005268997.2 1841 Missense Mutation ACA,ATA T481I XP_005269054.1

View Full Product Details