Product Details

SNP ID

rs34364313

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.2:222205149 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

GCAGTCGCTGCGTTAGAAAATTCAT[C/T]AGGAAAGGATTTAACTCTTAAGACC

Phenotype

MIM: 606597

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PAX3 PubMed Links

Additional Information

For this assay, SNP(s) [rs114443239] 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

PAX3

Gene Name

paired box 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000438.5		Intron			NP_000429.2
NM_001127366.2		Intron			NP_001120838.1
NM_013942.4		Intron			NP_039230.1
NM_181457.3		Intron			NP_852122.1
NM_181458.3		Intron			NP_852123.1
NM_181459.3		Intron			NP_852124.1
NM_181460.3		Intron			NP_852125.1
NM_181461.3		Intron			NP_852126.1

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