Product Details

SNP ID

rs150672120

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:51450920 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAATTAACTACATATTTCAAAATGC[A/G]TATCAGTGTATTAAAAGACTGAGAA

Phenotype

MIM: 612186

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DMXL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs68045371] 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

DMXL2

Gene Name

Dmx like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001174116.1		Intron			NP_001167587.1
NM_001174117.1		Intron			NP_001167588.1
NM_015263.3		Intron			NP_056078.2
XM_005254255.1		Intron			XP_005254312.1
XM_005254256.1		Intron			XP_005254313.1
XM_011521402.2		Intron			XP_011519704.1
XM_017022034.1		Intron			XP_016877523.1

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