Product Details

SNP ID

rs139319875

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:11948628 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTATGCTTGTAAAGTCTGTGGAAAA[A/G]CCTTTATTTTCCATTCAAGCATTCG

Phenotype

MIM: 194543

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ZNF69 PubMed Links

Additional Information

For this assay, SNP(s) [rs73509026] 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

ZNF69

Gene Name

zinc finger protein 69

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321163.1	756	Intron			NP_001308092.1
NM_021915.3	756	Intron			NP_068734.1
XM_006722873.3	756	Intron			XP_006722936.1
XM_006722874.3	756	Intron			XP_006722937.1
XM_017027231.1	756	Intron			XP_016882720.1

Gene

ZNF700

Gene Name

zinc finger protein 700

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271848.1	756	Missense Mutation	ACC,GCC	T205A	NP_001258777.1
NM_144566.2	756	Missense Mutation	ACC,GCC	T202A	NP_653167.1

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