Product Details

SNP ID

rs200017515

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64559141 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCACCCTCCTCTTGCAGTGGGAC[C/T]TGGTGTGCAGCTCCCAGGGCTTGAA

Phenotype

MIM: 607097

Polymorphism

C/T, Transition 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	799	Silent Mutation	CTG,TTG	L134L	NP_001294914.1
NM_018484.3	799	Silent Mutation	CTG,TTG	L134L	NP_060954.1
XM_011545167.1	799	Intron			XP_011543469.1

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