Product Details

SNP ID

rs61746632

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:69160643 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGGAGGGCTCTCCTCACACAAGC[G/T]CTTCCTTGCCGAGAGGCTGGAGCTG

Phenotype

MIM: 612134

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

GLCE PubMed Links

Additional Information

For this assay, SNP(s) [rs185082799,rs191936807] are located under a primer 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

GLCE

Gene Name

glucuronic acid epimerase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324091.1	89	UTR 5			NP_001311020.1
NM_001324092.1	89	UTR 5			NP_001311021.1
NM_001324093.1	89	UTR 5			NP_001311022.1
NM_001324094.1	89	UTR 5			NP_001311023.1
NM_015554.2	89	UTR 5			NP_056369.1
XM_005254298.3	89	UTR 5			XP_005254355.1
XM_017022073.1	89	Intron			XP_016877562.1
XM_017022074.1	89	Intron			XP_016877563.1

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