Product Details

SNP ID

rs12168831

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:25749688 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGGCATGCCACGTGGATGTCAGGG[C/T]GGTCGTCTTGTTCCCCATTACTCAA

Phenotype

MIM: 607295

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MYO18B PubMed Links

Additional Information

For this assay, SNP(s) [rs114989234] 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

MYO18B

Gene Name

myosin XVIIIB

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318245.1		Intron			NP_001305174.1
NM_032608.6		Intron			NP_115997.5
XM_011530458.2		Intron			XP_011528760.1
XM_011530459.2		Intron			XP_011528761.1
XM_011530460.2		Intron			XP_011528762.1
XM_011530461.2		Intron			XP_011528763.1
XM_011530464.2		Intron			XP_011528766.1
XM_011530465.2		Intron			XP_011528767.1
XM_011530466.2		Intron			XP_011528768.1
XM_017029012.1		Intron			XP_016884501.1
XM_017029013.1		Intron			XP_016884502.1
XM_017029014.1		Intron			XP_016884503.1
XM_017029015.1		Intron			XP_016884504.1
XM_017029016.1		Intron			XP_016884505.1
XM_017029017.1		Intron			XP_016884506.1

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