Product Details

SNP ID
rs201008586
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:36112524 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCTAATTCATGAGGCAACTCATGA[C/G]AGAACACAGCAACAGAAGTACTTAA
Phenotype
MIM: 608731
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC39A6 PubMed Links

Gene Details

Gene
SLC39A6
Gene Name
solute carrier family 39 member 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099406.1 2624 Missense Mutation TCT,TGT S359C NP_001092876.1
NM_012319.3 2624 Missense Mutation TCT,TGT S634C NP_036451.3
XM_011525900.1 2624 Missense Mutation TCT,TGT S634C XP_011524202.1
XM_011525901.1 2624 Missense Mutation TCT,TGT S634C XP_011524203.1

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