Product Details

SNP ID

rs10193644

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:62453658 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAATAAACAAAAACCTCTGTAGA[C/T]CTTTTTAAAATCTACCAGCAATGTT

Phenotype

MIM: 614950

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TMEM17 PubMed Links

Additional Information

For this assay, SNP(s) [rs114401627] 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

TMEM17

Gene Name

transmembrane protein 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198276.2		Intron			NP_938017.2
XM_011532693.2		Intron			XP_011530995.1
XM_011532694.2		Intron			XP_011530996.1
XM_017003575.1		Intron			XP_016859064.1

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