Product Details

SNP ID

rs456462

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:39800631 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTGGACATGGTTAGCCTTTTTGGA[A/G]CAGCCCCGGCTAAAGAGACTTGCTG

Phenotype

MIM: 606627

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DAAM2 PubMed Links

Additional Information

For this assay, SNP(s) [rs146618450] 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

DAAM2

Gene Name

dishevelled associated activator of morphogenesis 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001201427.1		Intron			NP_001188356.1
NM_015345.3		Intron			NP_056160.2
XM_006715039.3		Intron			XP_006715102.3
XM_006715040.3		Intron			XP_006715103.3
XM_006715042.2		Intron			XP_006715105.1
XM_006715043.2		Intron			XP_006715106.1
XM_006715045.3		Intron			XP_006715108.1
XM_006715046.3		Intron			XP_006715109.1
XM_017010630.1		Intron			XP_016866119.1

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