Product Details

SNP ID

rs76244995

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:44148799 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACTGACCTTCAAGGATGTGGCTG[G/T]GGTCTTCACTGAGGAGGAGCTGGGG

Phenotype

MIM: 604750

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

ZNF234 PubMed Links

Additional Information

For this assay, SNP(s) [rs2293587] 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

ZNF234

Gene Name

zinc finger protein 234

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144824.1	462	Missense Mutation	GGG,GTG	G15V	NP_001138296.1
NM_006630.2	462	Missense Mutation	GGG,GTG	G15V	NP_006621.1
XM_006722974.3	462	Missense Mutation	GGG,GTG	G15V	XP_006723037.1
XM_017026149.1	462	Missense Mutation	GGG,GTG	G15V	XP_016881638.1
XM_017026150.1	462	Missense Mutation	GGG,GTG	G15V	XP_016881639.1
XM_017026151.1	462	Missense Mutation	GGG,GTG	G15V	XP_016881640.1
XM_017026152.1	462	UTR 5			XP_016881641.1
XM_017026153.1	462	UTR 5			XP_016881642.1

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