Product Details

SNP ID

rs182279441

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:37903396 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCGCTGGGCGCCCTCCACTACCTG[A/G]CACTTTTCCTGCAACTCGGCGGCGC

Phenotype

MIM: 616537

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

VSTM2L PubMed Links

Additional Information

For this assay, SNP(s) [rs190346554] are located under a probe and SNP(s) [rs140613830] 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

VSTM2L

Gene Name

V-set and transmembrane domain containing 2 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080607.2	300	Missense Mutation	ACA,GCA	T16A	NP_542174.1
XM_011528530.1	300	Missense Mutation	ACA,GCA	T16A	XP_011526832.1

View Full Product Details