Product Details

SNP ID
rs199817296
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:49290199 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATTTCTTCCTTTTGAACCTCTTTA[C/G]TGGGTGTTAGCTGGTGACTTAGGGG
Phenotype
MIM: 607972
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC6A16 PubMed Links

Gene Details

Gene
SLC6A16
Gene Name
solute carrier family 6 member 16
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014037.2 2385 Missense Mutation ACT,AGT T712S NP_054756.2
XM_005258820.2 2385 Missense Mutation ACT,AGT T712S XP_005258877.1
XM_006723168.3 2385 Missense Mutation ACT,AGT T712S XP_006723231.1
XM_011526859.2 2385 Missense Mutation ACT,AGT T757S XP_011525161.2
XM_011526860.2 2385 Missense Mutation ACT,AGT T734S XP_011525162.1
XM_011526861.2 2385 Missense Mutation ACT,AGT T565S XP_011525163.1
XM_017026712.1 2385 Missense Mutation ACT,AGT T794S XP_016882201.1

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