Product Details

SNP ID

rs12310725

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:130873832 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCCTTGCTAACTGTACCATAGTTA[C/T]TCCTGCAGGTGAATATATAGGCTTT

Phenotype

MIM: 601179

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RAN PubMed Links

Additional Information

For this assay, SNP(s) [rs113400802] 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

RAN

Gene Name

RAN, member RAS oncogene family

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300796.1		Intron			NP_001287725.1
NM_001300797.1		Intron			NP_001287726.1
NM_006325.4		Intron			NP_006316.1
XM_017019772.1		Intron			XP_016875261.1
XM_017019773.1		Intron			XP_016875262.1

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