Product Details

SNP ID

rs12196682

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:38719920 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGCTGTTTCTTCTCCCTTACCACCA[C/G]AAAATGGAAACAAATACACAATGTT

Phenotype

MIM: 603337

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

DNAH8 PubMed Links

Additional Information

For this assay, SNP(s) [rs113223098] 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

DNAH8

Gene Name

dynein axonemal heavy chain 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206927.1		Intron			NP_001193856.1
XM_011514318.2		Intron			XP_011512620.1
XM_011514319.2		Intron			XP_011512621.1
XM_011514320.2		Intron			XP_011512622.1
XM_011514321.1		Intron			XP_011512623.1
XM_017010325.1		Intron			XP_016865814.1
XM_017010326.1		Intron			XP_016865815.1
XM_017010327.1		Intron			XP_016865816.1

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