Product Details

SNP ID

rs16852778

Assay Type

Functionally Tested

NCBI dbSNP Submissions

33

Location

Chr.1:204082313 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGCTCTGGAGACCCTGGCCAGGCT[C/T]CTCCAACCCATGGGAACCAGGCAGG

Phenotype

MIM: 604748

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SOX13 PubMed Links

Additional Information

For this assay, SNP(s) [rs112497628] 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

SOX13

Gene Name

SRY-box 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005686.2		Intron			NP_005677.2
XM_005245623.2		Intron			XP_005245680.1

View Full Product Details