Product Details

SNP ID

rs148202226

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64556041 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTGGAGCAAGCCGGAGGCGTGGG[A/C]CTCTTCCAGACCCTGCAGGTGCTCA

Phenotype

MIM: 607097

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC22A11 PubMed Links

Gene Details

Gene

SLC22A11

Gene Name

solute carrier family 22 member 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001307985.1	441	Silent Mutation	GGA,GGC	G14G	NP_001294914.1
NM_018484.3	441	Silent Mutation	GGA,GGC	G14G	NP_060954.1
XM_011545167.1	441	UTR 5			XP_011543469.1

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