Product Details

SNP ID

rs78036098

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:32159010 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTGGACATCTTCAGCATCTTCGGC[A/G]TCTTCGGGAGGCTGAGGTACTGCAT

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C22orf42 PubMed Links

Additional Information

For this assay, SNP(s) [rs12160688] 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

C22orf42

Gene Name

chromosome 22 open reading frame 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010859.1	749	Missense Mutation	ACG,ATG	T69M	NP_001010859.1
XM_011529922.2	749	Intron			XP_011528224.1
XM_017028629.1	749	Intron			XP_016884118.1
XM_017028630.1	749	Missense Mutation	ACG,ATG	T83M	XP_016884119.1
XM_017028631.1	749	Missense Mutation	ACG,ATG	T83M	XP_016884120.1
XM_017028632.1	749	Intron			XP_016884121.1

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