Product Details

SNP ID

rs3735706

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:100920800 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCAGCAAGTTTCAGTGGGATGGGG[A/G]GGGGGGGGCGTTTTCATATAAGTGC

Phenotype

MIM: 601288

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

YWHAZ PubMed Links

Additional Information

For this assay, SNP(s) [rs371130330] 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

YWHAZ

Gene Name

tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135699.1		Intron			NP_001129171.1
NM_001135700.1		Intron			NP_001129172.1
NM_001135701.1		Intron			NP_001129173.1
NM_001135702.1		Intron			NP_001129174.1
NM_003406.3		Intron			NP_003397.1
NM_145690.2		Intron			NP_663723.1
XM_005251061.3		Intron			XP_005251118.1
XM_005251063.3		Intron			XP_005251120.1
XM_011517290.2		Intron			XP_011515592.1
XM_017013810.1		Intron			XP_016869299.1
XM_017013811.1		Intron			XP_016869300.1
XM_017013812.1		Intron			XP_016869301.1

View Full Product Details