Product Details

SNP ID

rs13294100

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:17579692 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTTGCGGAGTCGGTGCACCCGGCT[G/T]TCCCGGGATGTGTTGGCATGAGCGG

Phenotype

MIM: 604465

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SH3GL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs184274313] 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

SH3GL2

Gene Name

SH3 domain containing GRB2 like 2, endophilin A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003026.3		Intron			NP_003017.1
XM_011518005.2		Intron			XP_011516307.1

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