Product Details

SNP ID

rs737182

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:110105777 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTGCCTTAAGGTCAGGCCTAAGAG[G/A]AGCCCTAATTTCTTCTCCCAGCCCC

Phenotype

MIM: 602022

Polymorphism

G/A, Transition Substitution

Allele Nomenclature

Literature Links

MALL PubMed Links

Additional Information

For this assay, SNP(s) [rs147645535] 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

MALL

Gene Name

mal, T-cell differentiation protein like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005434.4		Intron			NP_005425.1
XM_011511809.1		Intron			XP_011510111.1

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