Product Details

SNP ID

rs8112421

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:753715 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACAAAAAAAAATGCTGCTGGTTGG[A/T]GTAAAGGCAGCAGATCTAAATAATA

Phenotype

MIM: 615289 MIM: 608134

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

MISP PubMed Links

Additional Information

For this assay, SNP(s) [rs139343799] 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

MISP

Gene Name

mitotic spindle positioning

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173481.3		Intron			NP_775752.1
XM_011527685.2		Intron			XP_011525987.1
XM_011527686.2		Intron			XP_011525988.1

Gene

PALM

Gene Name

paralemmin

There are no transcripts associated with this gene.

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