Product Details

SNP ID

rs146664765

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:42564359 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGCCAGAGGTGCAGGCCATCGAC[A/C]GGAGCTTGCTGGAATGTTCGGCCGA

Phenotype

MIM: 609134

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

UBR2 PubMed Links

Additional Information

For this assay, SNP(s) [rs3749897] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

UBR2

Gene Name

ubiquitin protein ligase E3 component n-recognin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184801.1	338	Silent Mutation	AGG,CGG	R14R	NP_001171730.1
NM_015255.2	338	Silent Mutation	AGG,CGG	R14R	NP_056070.1
XM_005248965.4	338	Silent Mutation	AGG,CGG	R14R	XP_005249022.1
XM_005248966.3	338	Intron			XP_005249023.1
XM_011514438.2	338	UTR 5			XP_011512740.2
XM_011514439.1	338	Intron			XP_011512741.1
XM_011514440.1	338	Intron			XP_011512742.1
XM_011514441.2	338	Intron			XP_011512743.1
XM_017010594.1	338	UTR 5			XP_016866083.1
XM_017010595.1	338	UTR 5			XP_016866084.1
XM_017010596.1	338	Silent Mutation	AGG,CGG	R14R	XP_016866085.1
XM_017010597.1	338	UTR 5			XP_016866086.1

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