Product Details

SNP ID

rs8033877

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:77430782 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTCTAGAACTGTAAGAAAGTTAAT[C/T]TGTATTGCTTTAAGCCAATAGCTTT

Phenotype

MIM: 605534

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HMG20A PubMed Links

Additional Information

For this assay, SNP(s) [rs115924885] 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

HMG20A

Gene Name

high mobility group 20A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304504.1		Intron			NP_001291433.1
NM_001304505.1		Intron			NP_001291434.1
NM_018200.3		Intron			NP_060670.1
XM_011521158.2		Intron			XP_011519460.1

View Full Product Details