Product Details

SNP ID

rs465500

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:21444618 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGACAGTAGCCCGGGCTGTGAAACC[G/A]AATGCAAATCCCAGTTTCTCTATTT

Phenotype

MIM: 607712

Polymorphism

G/A, Transition Substitution

Allele Nomenclature

Literature Links

HIC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs138245684] 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

HIC2

Gene Name

hypermethylated in cancer 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015094.2		Intron			NP_055909.2
XM_011530007.2		Intron			XP_011528309.1
XM_011530008.2		Intron			XP_011528310.1
XM_011530009.2		Intron			XP_011528311.1
XM_011530010.2		Intron			XP_011528312.1
XM_017028669.1		Intron			XP_016884158.1

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