Product Details

SNP ID

rs6010987

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:63646322 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATGGAGGGGGACCAGGTGGGGGA[A/G]CCTCACAGGGGACTTTGGTCTGACT

Phenotype

MIM: 608362

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

STMN3 PubMed Links

Additional Information

For this assay, SNP(s) [rs113042387] are located under a probe 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

STMN3

Gene Name

stathmin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001276310.1		Intron			NP_001263239.1
NM_015894.3		Intron			NP_056978.2

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