Product Details

SNP ID
rs144269461
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:62977345 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTCACCAGTGGGCTCACGATGCT[G/T]CCCACTCGGGCCATGGTGCTGCCCA
Phenotype
MIM: 607582
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SLC22A6 PubMed Links

Gene Details

Gene
SLC22A6
Gene Name
solute carrier family 22 member 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004790.4 1737 Silent Mutation GGA,GGC G468G NP_004781.2
NM_153276.2 1737 Silent Mutation GGA,GGC G468G NP_695008.1
NM_153277.2 1737 Intron NP_695009.1
NM_153278.2 1737 Intron NP_695010.1
XM_017018562.1 1737 Silent Mutation GGA,GGC G469G XP_016874051.1

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