Product Details

SNP ID

rs4785983

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:5046752 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTTCCCTTTCTTCTACGTTATTT[A/C]TTGACTTTCTTCTACGTTATTTCTT

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

C16orf89 PubMed Links

Additional Information

For this assay, SNP(s) [rs76713390] are located under a probe 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

C16orf89

Gene Name

chromosome 16 open reading frame 89

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098514.2		Intron			NP_001091984.2
NM_152459.4		Intron			NP_689672.4
XM_005255143.3		Intron			XP_005255200.2
XM_011522392.2		Intron			XP_011520694.1
XM_017022972.1		Intron			XP_016878461.1
XM_017022973.1		Intron			XP_016878462.1
XM_017022974.1		Intron			XP_016878463.1

Gene

NAGPA-AS1

Gene Name

NAGPA antisense RNA 1

There are no transcripts associated with this gene.

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