Product Details

SNP ID

rs201104805

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:130342669 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCGCAGCTGGTGGGCTCCACTGC[C/T]GTGAGTGCTTCACCGTTTCTGACTA

Phenotype

MIM: 605571

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PIWIL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs11060834] 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

PIWIL1

Gene Name

piwi like RNA-mediated gene silencing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190971.1	292	Silent Mutation	GCC,GCT	A26A	NP_001177900.1
NM_004764.4	292	Silent Mutation	GCC,GCT	A26A	NP_004755.2
XM_011539002.2	292	Silent Mutation	GCC,GCT	A26A	XP_011537304.1
XM_011539003.2	292	Silent Mutation	GCC,GCT	A26A	XP_011537305.1
XM_011539004.2	292	Silent Mutation	GCC,GCT	A26A	XP_011537306.1
XM_011539005.1	292	Silent Mutation	GCC,GCT	A26A	XP_011537307.1
XM_011539006.2	292	Intron			XP_011537308.1
XM_017020229.1	292	Silent Mutation	GCC,GCT	A26A	XP_016875718.1

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