Product Details

SNP ID

rs193077243

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:3360113 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGTTACATTCTTGACACTTGTAAG[A/G]TTTCTCTCCAGTGTCAATGTTCTCA

Phenotype

MIM: 602187

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ZNF195 PubMed Links

Additional Information

For this assay, SNP(s) [rs62619253] 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

ZNF195

Gene Name

zinc finger protein 195

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130519.2	1414	Missense Mutation			NP_001123991.1
NM_001130520.2	1414	Missense Mutation			NP_001123992.1
NM_001242841.1	1414	Missense Mutation			NP_001229770.1
NM_001242842.1	1414	Missense Mutation			NP_001229771.1
NM_001242843.1	1414	Missense Mutation			NP_001229772.1
NM_001256823.1	1414	UTR 3			NP_001243752.1
NM_001256824.1	1414	Missense Mutation			NP_001243753.1
NM_001256825.1	1414	Missense Mutation			NP_001243754.1
NM_007152.4	1414	Missense Mutation			NP_009083.2
XM_006718306.1	1414	Missense Mutation			XP_006718369.1
XM_011520350.2	1414	Missense Mutation			XP_011518652.1
XM_011520351.2	1414	Missense Mutation			XP_011518653.1
XM_011520352.2	1414	Missense Mutation			XP_011518654.1
XM_011520354.2	1414	Intron			XP_011518656.2
XM_017018260.1	1414	Missense Mutation			XP_016873749.1
XM_017018261.1	1414	Missense Mutation			XP_016873750.1
XM_017018262.1	1414	Missense Mutation			XP_016873751.1
XM_017018263.1	1414	Missense Mutation			XP_016873752.1
XM_017018264.1	1414	Missense Mutation			XP_016873753.1
XM_017018265.1	1414	Missense Mutation			XP_016873754.1
XM_017018266.1	1414	Missense Mutation			XP_016873755.1
XM_017018267.1	1414	Missense Mutation			XP_016873756.1

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