Product Details

SNP ID
rs17221910
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:218382988 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAAGGGTCCCCAAAGGCTAAGCGG[A/G]TCCAGCTATGGTTCCATCTCCAGCC
Phenotype
MIM: 600266
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC11A1 PubMed Links

Gene Details

Gene
SLC11A1
Gene Name
solute carrier family 11 member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000578.3 639 Silent Mutation GGA,GGG G12G NP_000569.3
XM_005246793.3 639 Intron XP_005246850.1
XM_005246794.3 639 UTR 5 XP_005246851.1
XM_006712709.3 639 Intron XP_006712772.1
XM_006712710.3 639 Intron XP_006712773.1
XM_006712711.3 639 Intron XP_006712774.1
XM_011511684.2 639 UTR 5 XP_011509986.1
XM_011511685.2 639 Intron XP_011509987.1
XM_017004765.1 639 Silent Mutation GGA,GGG G12G XP_016860254.1
XM_017004766.1 639 UTR 5 XP_016860255.1
XM_017004767.1 639 Silent Mutation GGA,GGG G12G XP_016860256.1

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