Product Details

SNP ID
rs34570655
Assay Type
DME
NCBI dbSNP Submissions
NA
Location
Chr.6:160122002 on Build GRCh38
Set Membership
DME Validated Inventoried
Context Sequence [VIC/FAM]
TGGCTGGTTCCAGAAGCAAGCCTTC[C/G]TCATCTTATGCCTGCTGTCGGCTGC
Phenotype
MIM: 602607
Polymorphism
C/G, 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_003057.2 214 Missense Mutation CTC,GTC L23V NP_003048.1
NM_153187.1 214 Missense Mutation CTC,GTC L23V NP_694857.1
XM_005267102.4 214 Missense Mutation CTC,GTC L23V XP_005267159.1
XM_005267103.1 214 Missense Mutation CTC,GTC L23V XP_005267160.1
XM_005267104.4 214 Intron XP_005267161.1
XM_005267105.4 214 Intron XP_005267162.1
XM_006715552.1 214 Missense Mutation CTC,GTC L23V XP_006715615.1
XM_011536074.2 214 Intron XP_011534376.1

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