Product Details

SNP ID

rs2290368

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:151409959 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCACGCGTGAGTAAACAGCCGGAGC[C/T]GGGAAAGTCGAGCTCTGGCAGCGTC

Phenotype

MIM: 608952

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RIF1 PubMed Links

Additional Information

For this assay, SNP(s) [rs75732944] 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

RIF1

Gene Name

replication timing regulatory factor 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001177663.1	8	UTR 5			NP_001171134.1
NM_001177664.1	8	Intron			NP_001171135.1
NM_001177665.1	8	Intron			NP_001171136.1
NM_018151.4	8	UTR 5			NP_060621.3
XM_005246665.3	8	Intron			XP_005246722.1
XM_011511395.2	8	Intron			XP_011509697.1
XM_017004422.1	8	UTR 5			XP_016859911.1
XM_017004423.1	8	Intron			XP_016859912.1
XM_017004424.1	8	UTR 5			XP_016859913.1
XM_017004425.1	8	Intron			XP_016859914.1

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