Product Details

SNP ID

rs111966921

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:41183581 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCTCACTTCACTGAACAGCAGAG[A/G]CAACCGTTTCTAAGTTCCAGCCACT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CBWD6 PubMed Links

Additional Information

For this assay, SNP(s) [rs62557779] 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

CBWD6

Gene Name

COBW domain containing 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001085457.1		Intron			NP_001078926.1
XM_017015019.1		Intron			XP_016870508.1
XM_017015020.1		Intron			XP_016870509.1
XM_017015021.1		Intron			XP_016870510.1
XM_017015022.1		Intron			XP_016870511.1
XM_017015023.1		Intron			XP_016870512.1
XM_017015024.1		Intron			XP_016870513.1
XM_017015025.1		Intron			XP_016870514.1
XM_017015026.1		Intron			XP_016870515.1
XM_017015027.1		Intron			XP_016870516.1
XM_017015028.1		Intron			XP_016870517.1
XM_017015029.1		Intron			XP_016870518.1
XM_017015030.1		Intron			XP_016870519.1
XM_017015031.1		Intron			XP_016870520.1
XM_017015032.1		Intron			XP_016870521.1
XM_017015033.1		Intron			XP_016870522.1
XM_017015034.1		Intron			XP_016870523.1
XM_017015035.1		Intron			XP_016870524.1
XM_017015036.1		Intron			XP_016870525.1

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