Product Details

SNP ID
rs11877062
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.18:45727281 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTGAGAAAAAGTAAGGATGAATGGA[C/T]GGTCTTTGATTGGCGGCGCTGGTGA
Phenotype
MIM: 613868
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLC14A1 PubMed Links

Gene Details

Gene
SLC14A1
Gene Name
solute carrier family 14 member 1 (Kidd blood group)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001128588.3 208 Missense Mutation CGG,TGG R4W NP_001122060.3
NM_001146036.2 208 Intron NP_001139508.2
NM_001146037.1 208 Missense Mutation CGG,TGG R4W NP_001139509.1
NM_001308278.1 208 Intron NP_001295207.1
NM_001308279.1 208 Intron NP_001295208.1
NM_015865.6 208 Intron NP_056949.4
XM_005258329.1 208 Missense Mutation CGG,TGG R4W XP_005258386.1
XM_005258333.1 208 Intron XP_005258390.1
XM_006722526.3 208 Intron XP_006722589.1
XM_011526142.1 208 Intron XP_011524444.1
XM_011526144.1 208 Missense Mutation CGG,TGG R4W XP_011524446.1

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