Product Details

SNP ID

rs1019308

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:12212100 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

GGCAAGGGATTCCCAGTTTCTCACA[C/G]AGTCTGGCACTTGTCCAAACACCTA

Phenotype

MIM: 613413

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

TMEM106B PubMed Links

Additional Information

For this assay, SNP(s) [rs77287807] 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

TMEM106B

Gene Name

transmembrane protein 106B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134232.1		Intron			NP_001127704.1
NM_018374.3		Intron			NP_060844.2
XM_005249789.1		Intron			XP_005249846.1

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