Product Details

SNP ID

rs143239221

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:68304035 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCATGGGCCCCCTTACCAGCTCCCA[C/T]TCTTGGCTGTAGGGCTGCACGGAGA

Phenotype

MIM: 610087 MIM: 605641

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PRMT7 PubMed Links

Additional Information

For this assay, SNP(s) [rs11548855] 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

PRMT7

Gene Name

protein arginine methyltransferase 7

There are no transcripts associated with this gene.

Gene

SLC7A6

Gene Name

solute carrier family 7 member 6

There are no transcripts associated with this gene.

Gene

SLC7A6OS

Gene Name

solute carrier family 7 member 6 opposite strand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032178.2	708	Silent Mutation	GAA,GAG	E223E	NP_115554.2
XM_011523372.2	708	Silent Mutation	GAA,GAG	E223E	XP_011521674.1

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