Product Details

SNP ID
rs16856448
Assay Type
Functionally tested
NCBI dbSNP Submissions
44
Location
Chr.1:205914911 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTATCCCTATGTCCGTGACAGCCTG[A/G]CACCATCTGACACCGAGCCGTGTGG
Phenotype
MIM: 608481
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC26A9 PubMed Links

Gene Details

Gene
SLC26A9
Gene Name
solute carrier family 26 member 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_052934.3 2759 UTR 3 NP_443166.1
NM_134325.2 2759 Missense Mutation NP_599152.2
XM_011509121.2 2759 UTR 3 XP_011507423.1
XM_011509122.2 2759 UTR 3 XP_011507424.1
XM_011509124.2 2759 Intron XP_011507426.1

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