Product Details

SNP ID

rs7616319

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:126987708 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGTGTGAGGCTGGGAGCAGGACTGG[C/T]GGCTTGGATAGAGTGCTGAGAGTCA

Phenotype

MIM: 601055

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PLXNA1 PubMed Links

Additional Information

For this assay, SNP(s) [rs115813905] 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

PLXNA1

Gene Name

plexin A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032242.3		Intron			NP_115618.3
XM_011512908.2		Intron			XP_011511210.1
XM_011512909.1		Intron			XP_011511211.1

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