Product Details

SNP ID
rs10985085
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:120903019 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTGTTTCTCATGGGGGCTTGTTCTA[C/T]AAATCCCCCCTTGGGCTCAACACTC
Phenotype
MIM: 609740 MIM: 601711
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PHF19 PubMed Links
Additional Information
For this assay, SNP(s) [rs7037154] 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
PHF19
Gene Name
PHD finger protein 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001009936.2 3677 Intron NP_001009936.1
NM_001286840.1 3677 Intron NP_001273769.1
NM_001286842.1 3677 Intron NP_001273771.1
NM_001286843.1 3677 Intron NP_001273772.1
NM_015651.2 3677 Intron NP_056466.1
Gene
TRAF1
Gene Name
TNF receptor associated factor 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190945.1 3677 UTR 3 NP_001177874.1
NM_001190947.1 3677 UTR 3 NP_001177876.1
NM_005658.4 3677 UTR 3 NP_005649.1

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