Product Details

SNP ID
rs138075294
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:27255359 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCGCAGGCACTGGGCCATCTCCG[A/G]CTGATACTGCTCGACCTGCAGGGTG
Phenotype
MIM: 602878
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC30A3 PubMed Links

Gene Details

Gene
SLC30A3
Gene Name
solute carrier family 30 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318949.1 1163 Missense Mutation CCG,TCG P369S NP_001305878.1
NM_001318950.1 1163 Missense Mutation CCG,TCG P361S NP_001305879.1
NM_001318951.1 1163 Missense Mutation CCG,TCG P361S NP_001305880.1
NM_003459.4 1163 Missense Mutation CCG,TCG P374S NP_003450.2
XM_005264547.1 1163 Silent Mutation AGC,AGT S322S XP_005264604.1
XM_005264548.3 1163 Silent Mutation AGC,AGT S317S XP_005264605.1
XM_006712100.2 1163 Silent Mutation AGC,AGT S273S XP_006712163.1
XM_011533102.2 1163 Missense Mutation CCG,TCG P301S XP_011531404.1
XM_011533103.2 1163 Missense Mutation CCG,TCG P260S XP_011531405.1
XM_017004873.1 1163 Silent Mutation AGC,AGT S309S XP_016860362.1
XM_017004874.1 1163 Silent Mutation AGC,AGT S309S XP_016860363.1
XM_017004875.1 1163 Silent Mutation AGC,AGT S300S XP_016860364.1

View Full Product Details