Product Details

SNP ID

rs1546258

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:26560414 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCGTCTTATTGTTGTCCTATTCCT[A/G]TTTCTTTCTTCAGAGGTAACCATAA

Phenotype

MIM: 605068

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

WASF3 PubMed Links

Additional Information

For this assay, SNP(s) [rs200568667] 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

WASF3

Gene Name

WAS protein family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291965.1		Intron			NP_001278894.1
NM_006646.5		Intron			NP_006637.2
XM_011534889.1		Intron			XP_011533191.1
XM_011534890.1		Intron			XP_011533192.1

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