Product Details

SNP ID

rs11503450

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:103054143 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAAGAAATCTTACTGGGATTTTGAT[A/G]GTGATTGCATTGAACCTATAAATCA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

C12orf42 PubMed Links

Additional Information

For this assay, SNP(s) [rs139019855] 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

C12orf42

Gene Name

chromosome 12 open reading frame 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099336.2		Intron			NP_001092806.1
NM_001278419.1		Intron			NP_001265348.1
NM_001278420.1		Intron			NP_001265349.1
NM_198521.3		Intron			NP_940923.2
XM_006719377.3		Intron			XP_006719440.1
XM_011538291.1		Intron			XP_011536593.1
XM_011538292.2		Intron			XP_011536594.1
XM_011538293.2		Intron			XP_011536595.1
XM_011538294.2		Intron			XP_011536596.1
XM_011538295.1		Intron			XP_011536597.1
XM_011538297.2		Intron			XP_011536599.1
XM_011538300.1		Intron			XP_011536602.1
XM_011538305.1		Intron			XP_011536607.1
XM_011538306.1		Intron			XP_011536608.1
XM_011538308.2		Intron			XP_011536610.1
XM_011538312.2		Intron			XP_011536614.1
XM_011538315.2		Intron			XP_011536617.1
XM_017019276.1		Intron			XP_016874765.1
XM_017019277.1		Intron			XP_016874766.1
XM_017019278.1		Intron			XP_016874767.1
XM_017019279.1		Intron			XP_016874768.1
XM_017019280.1		Intron			XP_016874769.1
XM_017019281.1		Intron			XP_016874770.1

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