Product Details

SNP ID

rs11656157

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:11961793 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTCTGCCTGGGTGCCATGAGCCAG[A/G]GGTCTCTGAGGCCAGGTGTTTTCAG

Phenotype

MIM: 603330 MIM: 194524

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DNAH9 PubMed Links

Additional Information

For this assay, SNP(s) [rs143970860] 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

DNAH9

Gene Name

dynein axonemal heavy chain 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001372.3		Intron			NP_001363.2
NM_004662.2		Intron			NP_004653.2
XM_011523703.1		Intron			XP_011522005.1
XM_017024292.1		Intron			XP_016879781.1
XM_017024293.1		Intron			XP_016879782.1
XM_017024294.1		Intron			XP_016879783.1
XM_017024295.1		Intron			XP_016879784.1

Gene

ZNF18

Gene Name

zinc finger protein 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303281.1		Intron			NP_001290210.1
NM_001303282.1		Intron			NP_001290211.1
NM_144680.3		Intron			NP_653281.2
XM_011524002.2		Intron			XP_011522304.1
XM_017025006.1		Intron			XP_016880495.1
XM_017025007.1		Intron			XP_016880496.1
XM_017025008.1		Intron			XP_016880497.1
XM_017025009.1		Intron			XP_016880498.1
XM_017025010.1		Intron			XP_016880499.1
XM_017025011.1		Intron			XP_016880500.1

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