Product Details

SNP ID
rs144140450
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:62993592 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCGGGGACACCATGCTTCCCACG[C/T]GGGTCCACAGGTTACTTACGCCCAT
Phenotype
MIM: 607582 MIM: 607581
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC22A6 PubMed Links

Gene Details

Gene
SLC22A6
Gene Name
solute carrier family 22 member 6
There are no transcripts associated with this gene.

Gene
SLC22A8
Gene Name
solute carrier family 22 member 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184732.1 1503 Missense Mutation CAC,CGC H454R NP_001171661.1
NM_001184733.1 1503 Missense Mutation CAC,CGC H363R NP_001171662.1
NM_001184736.1 1503 Missense Mutation CAC,CGC H331R NP_001171665.1
NM_004254.3 1503 Missense Mutation CAC,CGC H454R NP_004245.2
XM_011545364.1 1503 Missense Mutation CAC,CGC H331R XP_011543666.1

View Full Product Details