Product Details

SNP ID
rs116401889
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:42417950 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTGCGGGAGCGGATCCAGCCCAC[A/G]GCCACCACCGAGCCCACCTGTGGGA
Phenotype
MIM: 158378
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC20A2 PubMed Links

Gene Details

Gene
SLC20A2
Gene Name
solute carrier family 20 member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001257180.1 2244 Silent Mutation GCC,GCT A604A NP_001244109.1
NM_001257181.1 2244 Silent Mutation GCC,GCT A604A NP_001244110.1
NM_006749.4 2244 Silent Mutation GCC,GCT A604A NP_006740.1
XM_005273613.3 2244 Silent Mutation GCC,GCT A604A XP_005273670.1
XM_005273615.3 2244 UTR 3 XP_005273672.1
XM_006716390.3 2244 Silent Mutation GCC,GCT A557A XP_006716453.1
XM_006716391.3 2244 Silent Mutation GCC,GCT A467A XP_006716454.1
XM_017013748.1 2244 Silent Mutation GCC,GCT A604A XP_016869237.1
XM_017013749.1 2244 Silent Mutation GCC,GCT A557A XP_016869238.1
XM_017013750.1 2244 Silent Mutation GCC,GCT A467A XP_016869239.1
XM_017013751.1 2244 Silent Mutation GCC,GCT A467A XP_016869240.1
XM_017013752.1 2244 Silent Mutation GCC,GCT A467A XP_016869241.1

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