Product Details

SNP ID

rs41313272

Assay Type

Functionally Tested

NCBI dbSNP Submissions

38

Location

Chr.1:67093073 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCAGTGGCGTTACATTATTTAGTT[C/T]ATATATATATTTAAAAGGCTTTGAG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C1orf141 PubMed Links

Additional Information

For this assay, SNP(s) [rs41299551,rs567792598] are located under a probe 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

C1orf141

Gene Name

chromosome 1 open reading frame 141

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001276351.1	1368	Missense Mutation	AAA,GAA	K379E	NP_001263280.1
NM_001276352.1	1368	UTR 3			NP_001263281.1
XM_011541465.2	1368	Missense Mutation	AAA,GAA	K450E	XP_011539767.1
XM_011541466.2	1368	Missense Mutation	AAA,GAA	K450E	XP_011539768.1
XM_011541467.1	1368	Missense Mutation	AAA,GAA	K437E	XP_011539769.1
XM_011541469.1	1368	Missense Mutation	AAA,GAA	K312E	XP_011539771.1
XM_011541472.1	1368	Intron			XP_011539774.1
XM_011541473.2	1368	Intron			XP_011539775.1
XM_011541475.1	1368	Intron			XP_011539777.1
XM_017001276.1	1368	Missense Mutation	AAA,GAA	K450E	XP_016856765.1
XM_017001277.1	1368	Intron			XP_016856766.1

View Full Product Details