Product Details

SNP ID

rs78779496

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:168293869 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCTGTGACTGGTCAGTCAATGCA[A/G]CCCCCAGCTTGGTGTAGTGCTCTGT

Phenotype

MIM: 608966

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DACT2 PubMed Links

Additional Information

For this assay, SNP(s) [rs33979593] 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

DACT2

Gene Name

dishevelled binding antagonist of beta catenin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286350.1	989	Intron			NP_001273279.1
NM_001286351.1	989	UTR 3			NP_001273280.1
NM_214462.4	989	Intron			NP_999627.2
XM_011535507.2	989	Intron			XP_011533809.1

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