Product Details

SNP ID
rs201620887
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:45727413 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTGGCCCTGGCAGATGGGTCGCAG[A/G]AACAGGTATGCTTCCTTCGTGCAGC
Phenotype
MIM: 613868
Polymorphism
A/G, 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_001128588.3 340 Missense Mutation AAA,GAA K48E NP_001122060.3
NM_001146036.2 340 UTR 5 NP_001139508.2
NM_001146037.1 340 Missense Mutation AAA,GAA K48E NP_001139509.1
NM_001308278.1 340 Intron NP_001295207.1
NM_001308279.1 340 Intron NP_001295208.1
NM_015865.6 340 Intron NP_056949.4
XM_005258329.1 340 Missense Mutation AAA,GAA K48E XP_005258386.1
XM_005258333.1 340 Intron XP_005258390.1
XM_006722526.3 340 Intron XP_006722589.1
XM_011526142.1 340 Intron XP_011524444.1
XM_011526144.1 340 Missense Mutation AAA,GAA K48E XP_011524446.1

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