Product Details

SNP ID

rs2757589

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:163422186 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCTTACAATTAGCAAGAAAAGGAC[C/T]GCACTTAATGTTTTCGTCTTCAGTT

Phenotype

MIM: 615930 MIM: 609590

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CAHM PubMed Links

Additional Information

For this assay, SNP(s) [rs150200739] 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

CAHM

Gene Name

colon adenocarcinoma hypermethylated (non-protein coding)

There are no transcripts associated with this gene.

Gene

QKI

Gene Name

QKI, KH domain containing RNA binding

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001301085.1		Intron			NP_001288014.1
NM_006775.2		Intron			NP_006766.1
NM_206853.2		Intron			NP_996735.1
NM_206854.2		Intron			NP_996736.1
NM_206855.2		Intron			NP_996737.1
XM_011536258.2		Intron			XP_011534560.1
XM_011536259.2		Intron			XP_011534561.1
XM_011536260.2		Intron			XP_011534562.1
XM_011536261.1		Intron			XP_011534563.1
XM_017011502.1		Intron			XP_016866991.1
XM_017011503.1		Intron			XP_016866992.1
XM_017011504.1		Intron			XP_016866993.1

View Full Product Details