Product Details

SNP ID

rs34458044

Assay Type

Functionally Tested

NCBI dbSNP Submissions

36

Location

Chr.1:245753113 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGATGCTGAATGCATCACCAGTAGC[A/C]AAGGGGAACAGGGGCAACCCTCAGG

Phenotype

MIM: 608783

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SMYD3 PubMed Links

Additional Information

For this assay, SNP(s) [rs112693109] 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

SMYD3

Gene Name

SET and MYND domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001167740.1		Intron			NP_001161212.1
NM_022743.2		Intron			NP_073580.1
XM_011544253.1		Intron			XP_011542555.1
XM_011544254.2		Intron			XP_011542556.1
XM_011544257.1		Intron			XP_011542559.1
XM_011544258.2		Intron			XP_011542560.1
XM_011544259.2		Intron			XP_011542561.1
XM_011544260.1		Intron			XP_011542562.1
XM_011544261.2		Intron			XP_011542563.1
XM_017002094.1		Intron			XP_016857583.1
XM_017002095.1		Intron			XP_016857584.1

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