Product Details

SNP ID

rs11038297

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:45104915 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGGACCATCTCCTCCTCCTGCATC[C/T]TGGACAGGGGTCATGTAATTCCACC

Phenotype

MIM: 616347

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PRDM11 PubMed Links

Additional Information

For this assay, SNP(s) [rs79182289] 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

PRDM11

Gene Name

PR domain 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256695.1		Intron			NP_001243624.1
NM_001256696.1		Intron			NP_001243625.1
XM_011520222.2		Intron			XP_011518524.1
XM_011520223.2		Intron			XP_011518525.1
XM_011520224.2		Intron			XP_011518526.1
XM_011520225.2		Intron			XP_011518527.1
XM_011520226.2		Intron			XP_011518528.1
XM_011520227.2		Intron			XP_011518529.1
XM_011520228.2		Intron			XP_011518530.1
XM_011520230.2		Intron			XP_011518532.1
XM_011520231.2		Intron			XP_011518533.1
XM_017018024.1		Intron			XP_016873513.1

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