Product Details

SNP ID

rs11707321

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.3:44980604 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

CCTGCTGCAGTGAAAGTCATTTCTT[C/T]CATTTCCTCAGTAGGGATCCAGAGA

Phenotype

MIM: 606488

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

EXOSC7 PubMed Links

Additional Information

For this assay, SNP(s) [rs28427135] 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

EXOSC7

Gene Name

exosome component 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015004.3		Intron			NP_055819.2
XM_017005930.1		Intron			XP_016861419.1

Gene

ZDHHC3

Gene Name

zinc finger DHHC-type containing 3

There are no transcripts associated with this gene.

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