Product Details

SNP ID
rs201731508
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:160122279 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTAGCCTGGCCACCAACAGGAGCC[A/C]CCTGCCGCTGGGTCCCTGCCAGGAT
Phenotype
MIM: 602607
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC22A1 PubMed Links

Gene Details

Gene
SLC22A1
Gene Name
solute carrier family 22 member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003057.2 491 Missense Mutation CAC,CCC H115P NP_003048.1
NM_153187.1 491 Missense Mutation CAC,CCC H115P NP_694857.1
XM_005267102.4 491 Missense Mutation CAC,CCC H115P XP_005267159.1
XM_005267103.1 491 Missense Mutation CAC,CCC H115P XP_005267160.1
XM_005267104.4 491 Intron XP_005267161.1
XM_005267105.4 491 Intron XP_005267162.1
XM_006715552.1 491 Missense Mutation CAC,CCC H115P XP_006715615.1
XM_011536074.2 491 Intron XP_011534376.1

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