Product Details

SNP ID
rs1049358
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.12:46183288 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
TTAATAAAACAGTAGTGTGGTACAT[A/G]TATTGGACTCAGATGAAGTCTAAAG
Phenotype
MIM: 608490
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC38A1 PubMed Links

Gene Details

Gene
SLC38A1
Gene Name
solute carrier family 38 member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001077484.1 7915 UTR 3 NP_001070952.1
NM_001278387.1 7915 UTR 3 NP_001265316.1
NM_001278388.1 7915 UTR 3 NP_001265317.1
NM_001278389.1 7915 UTR 3 NP_001265318.1
NM_001278390.1 7915 Intron NP_001265319.1
NM_030674.3 7915 UTR 3 NP_109599.3
XM_011538784.2 7915 Intron XP_011537086.1
XM_011538786.2 7915 Intron XP_011537088.1
XM_011538787.2 7915 Intron XP_011537089.1
XM_017019990.1 7915 Intron XP_016875479.1

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