Product Details

SNP ID

rs1224329

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:37212461 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CATTCCCAGACGGACAGGTAGTCAT[A/G]AGTTCACTGCAATGGTGGAGCAGAG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TMEM217 PubMed Links

Additional Information

For this assay, SNP(s) [rs74359974] 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

TMEM217

Gene Name

transmembrane protein 217

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001162900.1	1740	Intron			NP_001156372.1
NM_001286401.1	1740	UTR 3			NP_001273330.1
NM_145316.3	1740	UTR 3			NP_660359.2
XM_011514362.1	1740	Intron			XP_011512664.1
XM_011514363.2	1740	Intron			XP_011512665.1
XM_011514364.2	1740	Intron			XP_011512666.1
XM_011514365.2	1740	Intron			XP_011512667.1
XM_011514366.2	1740	Intron			XP_011512668.1
XM_011514367.2	1740	Intron			XP_011512669.1
XM_011514369.2	1740	Missense Mutation	TCA,TTA	S170L	XP_011512671.1
XM_011514370.2	1740	Missense Mutation	TCA,TTA	S170L	XP_011512672.1

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