Product Details

SNP ID

rs77417309

Assay Type

Functionally Tested

NCBI dbSNP Submissions

2

Location

Chr.1:26320192 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAGATACAAACTGGACTCTCAGGA[A/C]AAAACGACACCAGCCAAACCAGCAG

Phenotype

MIM: 114280 MIM: 609151

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

AIM1L PubMed Links

Additional Information

For this assay, SNP(s) [rs1071849,rs17645] 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

AIM1L

Gene Name

absent in melanoma 1-like

There are no transcripts associated with this gene.

Gene

CD52

Gene Name

CD52 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001803.2	174	Missense Mutation	AAA,CAA	K26Q	NP_001794.2

Gene

UBXN11

Gene Name

UBX domain protein 11

There are no transcripts associated with this gene.

View Full Product Details