Product Details

SNP ID

rs7127456

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:45810744 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCTCGTCCTCATCCCTCTTCCTC[A/G]CCCTTCCCCACTCCTCCTCTCCCCA

Phenotype

MIM: 605881

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC35C1 PubMed Links

Additional Information

For this assay, SNP(s) [rs111402424] 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

SLC35C1

Gene Name

solute carrier family 35 member C1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145265.1		Intron			NP_001138737.1
NM_001145266.1		Intron			NP_001138738.1
NM_018389.4		Intron			NP_060859.4
XM_011520202.2		Intron			XP_011518504.1
XM_011520203.2		Intron			XP_011518505.1

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