Product Details

SNP ID
rs140682366
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:151316858 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGGAGTTGGAAAAGGGGTGAGAGT[C/T]TTCTGACTTGAGCAGCTCGTCCAGG
Phenotype
MIM: 608331
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC36A2 PubMed Links

Gene Details

Gene
SLC36A2
Gene Name
solute carrier family 36 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_181776.2 1449 Missense Mutation AAC,GAC N471D NP_861441.2
XM_005268377.3 1449 Intron XP_005268434.1
XM_006714756.3 1449 Missense Mutation AAC,GAC N438D XP_006714819.1
XM_017009083.1 1449 Intron XP_016864572.1
XM_017009084.1 1449 Missense Mutation AAC,GAC N273D XP_016864573.1

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