Product Details

SNP ID

rs12212727

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:135188293 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTTTGGCACCAAGGTTTAAAATT[C/T]TGAAGACCTTTCTTGACTTATCACA

Phenotype

MIM: 189990

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MYB PubMed Links

Additional Information

For this assay, SNP(s) [rs76250521] 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

MYB

Gene Name

MYB proto-oncogene, transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130172.1		Intron			NP_001123644.1
NM_001130173.1		Intron			NP_001123645.1
NM_001161656.1		Intron			NP_001155128.1
NM_001161657.1		Intron			NP_001155129.1
NM_001161658.1		Intron			NP_001155130.1
NM_001161659.1		Intron			NP_001155131.1
NM_001161660.1		Intron			NP_001155132.1
NM_005375.3		Intron			NP_005366.2

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