Product Details

SNP ID

rs13106599

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:25706111 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTTCTGTCTTCACCTCTCACCCT[C/T]GGCCCCCTCCAATAGGCTTGGCCTA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SEL1L3 PubMed Links

Additional Information

For this assay, SNP(s) [rs150263273] 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

SEL1L3

Gene Name

SEL1L family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001297592.1		Intron			NP_001284521.1
NM_001297594.1		Intron			NP_001284523.1
NM_015187.4		Intron			NP_056002.2
XM_011513819.2		Intron			XP_011512121.2
XM_017007923.1		Intron			XP_016863412.1

View Full Product Details