Product Details

SNP ID
rs201455367
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:111087995 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGATGCTGGCGGCCATGTGGTGCAA[A/C]GGGTCGGTGTTCGGCATCCAGAACG
Phenotype
MIM: 607550
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC16A10 PubMed Links

Gene Details

Gene
SLC16A10
Gene Name
solute carrier family 16 member 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018593.4 493 Missense Mutation AAA,AAC K81N NP_061063.2
XM_006715329.2 493 Missense Mutation AAA,AAC K81N XP_006715392.1
XM_011535422.2 493 Missense Mutation AAA,AAC K81N XP_011533724.1
XM_017010237.1 493 Intron XP_016865726.1

View Full Product Details