Product Details

SNP ID

rs610149

Assay Type

Functionally Tested

NCBI dbSNP Submissions

26

Location

Chr.1:84929933 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAAGAGCCAGGGAGAGGTTTTTTT[A/T]AAAAAAAAAAAAGGTAATGAAGGAA

Phenotype

MIM: 607399

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

MCOLN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs550754228] are located under a probe 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

MCOLN2

Gene Name

mucolipin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153259.3		Intron			NP_694991.2
XM_005270719.3		Intron			XP_005270776.1
XM_006710552.2		Intron			XP_006710615.1
XM_011541187.2		Intron			XP_011539489.1
XM_011541188.2		Intron			XP_011539490.1
XM_017000923.1		Intron			XP_016856412.1

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