Product Details

SNP ID

rs1208606

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:37952139 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCCCAACTCATCTTACTTCTCAGC[A/C]TTCCTCTTCTTTGTGTGTGTCTTCT

Phenotype

MIM: 194528

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

ZNF25 PubMed Links

Additional Information

For this assay, SNP(s) [rs147942111] 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

ZNF25

Gene Name

zinc finger protein 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005252384.2	1702	Missense Mutation	AAG,AAT	K453N	XP_005252441.1
XM_005252385.2	1702	Missense Mutation	AAG,AAT	K453N	XP_005252442.1
XM_005252386.2	1702	Missense Mutation	AAG,AAT	K453N	XP_005252443.1
XM_011519352.2	1702	Missense Mutation	AAG,AAT	K457N	XP_011517654.1
XM_011519353.2	1702	Missense Mutation	AAG,AAT	K457N	XP_011517655.1
XM_011519354.2	1702	Missense Mutation	AAG,AAT	K457N	XP_011517656.1
XM_011519355.2	1702	Missense Mutation	AAG,AAT	K457N	XP_011517657.1
XM_011519356.2	1702	Missense Mutation	AAG,AAT	K417N	XP_011517658.1
XM_017015837.1	1702	Missense Mutation	AAG,AAT	K417N	XP_016871326.1
XM_017015838.1	1702	Missense Mutation	AAG,AAT	K417N	XP_016871327.1

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