Product Details

SNP ID

rs139243712

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:35939456 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATCCTCCCGTTGCTCCTGTGCCTG[C/G]TGCCGCTGGCCCCTGCCTCATCCCC

Phenotype

MIM: 612809

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

LOC105372383 PubMed Links

Additional Information

For this assay, SNP(s) [rs2242590] 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

LOC105372383

Gene Name

uncharacterized LOC105372383

There are no transcripts associated with this gene.

Gene

LRFN3

Gene Name

leucine rich repeat and fibronectin type III domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024509.1	483	Missense Mutation	CTG,GTG	L11V	NP_078785.1
XM_017027302.1	483	Missense Mutation	CTG,GTG	L11V	XP_016882791.1

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