Product Details

SNP ID

rs76129882

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:59639387 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGGAGCAGTGACAGGCCAAACTA[C/T]GAGAAAAGACAGAGGGAATCAAACT

Phenotype

MIM: 614660

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PATL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs77539333] 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

PATL1

Gene Name

PAT1 homolog 1, processing body mRNA decay factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152716.2		Intron			NP_689929.2
XM_005273833.4		Intron			XP_005273890.1
XM_005273834.1		Intron			XP_005273891.1
XM_011544811.2		Intron			XP_011543113.1
XM_017017339.1		Intron			XP_016872828.1

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