Product Details

SNP ID: rs202087879
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.19:16680015 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCGAACTGTCCCGGCGCCACCCCAT[C/T]GCGTCCTGGCTGTGCGCCATGCTGC
Phenotype: MIM: 611235
Polymorphism: C/T, Transition Substitution
Allele Nomenclature
Literature Links: TMEM38A PubMed Links
Additional Information: For this assay, SNP(s) [rs730120] 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024074.2	247	Silent Mutation	ATC,ATT	I52I	NP_076979.1