Product Details

SNP ID
rs7896053
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:15096616 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACTTTGCAGCGACTCCGATGGTAGC[C/T]TGAGTCTCCATTGCTTGGAGCAGCC
Phenotype
MIM: 603801 MIM: 606116
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
ACBD7 PubMed Links
Additional Information
For this assay, SNP(s) [rs77851121] 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
ACBD7
Gene Name
acyl-CoA binding domain containing 7
There are no transcripts associated with this gene.

Gene
C10orf111
Gene Name
chromosome 10 open reading frame 111
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153244.1 483 Missense Mutation AAG,AGG K70R NP_694976.1
Gene
NMT2
Gene Name
N-myristoyltransferase 2
There are no transcripts associated with this gene.

Gene
RPP38
Gene Name
ribonuclease P/MRP subunit p38
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001097590.2 483 Intron NP_001091059.1
NM_001265601.1 483 Intron NP_001252530.1
NM_006414.4 483 Intron NP_006405.2
NM_183005.4 483 Intron NP_892117.1
XM_006717363.1 483 Intron XP_006717426.1
XM_006717364.3 483 Intron XP_006717427.1
XM_011519293.1 483 Intron XP_011517595.1
XM_017015479.1 483 Intron XP_016870968.1
XM_017015480.1 483 Intron XP_016870969.1
XM_017015481.1 483 Intron XP_016870970.1

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