Product Details

SNP ID

rs141159367

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64556004 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGCCGAGGCAGCTCTGTTCATGG[C/T]GTTCTCGAAGCTCTTGGAGCAAGCC

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	404	Missense Mutation	GCG,GTG	A2V	NP_001294914.1
NM_018484.3	404	Missense Mutation	GCG,GTG	A2V	NP_060954.1
XM_011545167.1	404	UTR 5			XP_011543469.1

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