Product Details

SNP ID
rs142260441
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:10923332 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACTGCGGCAAGGTAGGGGACAGCG[C/T]GATGTTTGAGGGCAGAGATGTGATT
Phenotype
MIM: 603934
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C19orf52 PubMed Links
Additional Information
For this assay, SNP(s) [rs17850995] 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
C19orf52
Gene Name
chromosome 19 open reading frame 52
There are no transcripts associated with this gene.

Gene
CARM1
Gene Name
coactivator associated arginine methyltransferase 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_199141.1 980 Intron NP_954592.1
XM_005259708.4 980 Intron XP_005259765.1
XM_011527638.2 980 Intron XP_011525940.1
Gene
YIPF2
Gene Name
Yip1 domain family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321439.1 980 Missense Mutation NP_001308368.1
NM_001321440.1 980 Missense Mutation NP_001308369.1
NM_024029.4 980 Missense Mutation NP_076934.1
XM_011528270.2 980 Missense Mutation XP_011526572.1
XM_011528271.2 980 Missense Mutation XP_011526573.1

View Full Product Details