Product Details

SNP ID

rs12293073

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:581279 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTAGGGCTCACCCTTCACGTGCTG[C/T]GGCGGTGGATGTGACACTGGGACAC

Phenotype

MIM: 611780

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LOC143666 PubMed Links

Additional Information

For this assay, SNP(s) [rs111406154] 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

LOC143666

Gene Name

uncharacterized LOC143666

There are no transcripts associated with this gene.

Gene

PHRF1

Gene Name

PHD and ring finger domains 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286581.1		Intron			NP_001273510.1
NM_001286582.1		Intron			NP_001273511.1
NM_001286583.1		Intron			NP_001273512.1
NM_020901.3		Intron			NP_065952.2
XM_005253025.4		Intron			XP_005253082.1
XM_005253027.3		Intron			XP_005253084.1
XM_011520236.2		Intron			XP_011518538.1
XM_011520237.2		Intron			XP_011518539.1

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