Product Details

SNP ID

rs12108989

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:110387282 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTAGTTACCTCTCACTTTGTACTT[C/T]ATTATAGCACTCTTTCTCTCAGTTG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TMEM232 PubMed Links

Additional Information

For this assay, SNP(s) [rs77971917] 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

TMEM232

Gene Name

transmembrane protein 232

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039763.3		Intron			NP_001034852.3
XM_006714670.3		Intron			XP_006714733.1
XM_011543552.2		Intron			XP_011541854.1
XM_011543553.2		Intron			XP_011541855.1
XM_011543555.2		Intron			XP_011541857.1
XM_011543556.1		Intron			XP_011541858.1
XM_011543557.2		Intron			XP_011541859.1
XM_011543559.2		Intron			XP_011541861.1
XM_011543560.2		Intron			XP_011541862.1
XM_011543561.2		Intron			XP_011541863.1
XM_011543563.2		Intron			XP_011541865.1
XM_011543564.2		Intron			XP_011541866.1
XM_011543565.2		Intron			XP_011541867.1
XM_011543566.2		Intron			XP_011541868.1
XM_011543567.2		Intron			XP_011541869.1
XM_017009704.1		Intron			XP_016865193.1
XM_017009705.1		Intron			XP_016865194.1
XM_017009706.1		Intron			XP_016865195.1
XM_017009707.1		Intron			XP_016865196.1

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