Product Details

SNP ID

rs7621631

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:169794357 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCTACAGATTTAGGCTAAAACAGA[A/C]AATTCCATAGTATTGGATGCGGACC

Phenotype

MIM: 606042

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

LRRC34 PubMed Links

Additional Information

For this assay, SNP(s) [rs7643115] 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

LRRC34

Gene Name

leucine rich repeat containing 34

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001172779.1		Intron			NP_001166250.1
NM_001172780.1		Intron			NP_001166251.1
NM_153353.4		Intron			NP_699184.2
XM_006713508.3		Intron			XP_006713571.1
XM_011512442.2		Intron			XP_011510744.1
XM_017005746.1		Intron			XP_016861235.1

Gene

MYNN

Gene Name

myoneurin

There are no transcripts associated with this gene.

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