Product Details

SNP ID
rs143126713
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:10627950 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCATGGAGACCCTCGAAAGGTGA[C/T]CTACCCCACTGACAGCCGGGGCGAG
Phenotype
MIM: 606106
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC44A2 PubMed Links

Gene Details

Gene
SLC44A2
Gene Name
solute carrier family 44 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145056.1 330 Missense Mutation ACC,ATC T62I NP_001138528.1
NM_020428.3 330 Missense Mutation ACC,ATC T64I NP_065161.3
XM_005259997.1 330 Missense Mutation ACC,ATC T64I XP_005260054.1
XM_005259999.1 330 Missense Mutation ACC,ATC T62I XP_005260056.1

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