Product Details

SNP ID
rs1875682
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:126008047 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCAGCAGACCCTGCAGGGGTCTGGC[A/C]CTGCCCACCCACCGTTGGGGAGGCA
Phenotype
MIM: 610803
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
SLC41A3 PubMed Links

Gene Details

Gene
SLC41A3
Gene Name
solute carrier family 41 member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008485.1 Intron NP_001008485.1
NM_001008486.1 Intron NP_001008486.1
NM_001008487.1 Intron NP_001008487.1
NM_001164475.1 Intron NP_001157947.1
NM_017836.3 Intron NP_060306.3
XM_005247559.1 Intron XP_005247616.1
XM_005247562.1 Intron XP_005247619.1
XM_005247563.2 Intron XP_005247620.1
XM_005247564.1 Intron XP_005247621.1
XM_005247565.2 Intron XP_005247622.1
XM_006713681.2 Intron XP_006713744.1
XM_011512945.1 Intron XP_011511247.1
XM_017006705.1 Intron XP_016862194.1
XM_017006706.1 Intron XP_016862195.1
XM_017006707.1 Intron XP_016862196.1
XM_017006708.1 Intron XP_016862197.1
XM_017006709.1 Intron XP_016862198.1

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