Product Details

SNP ID

rs150496983

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:15096635 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTAGCCTGAGTCTCCATTGCTTGG[A/T]GCAGCCACAGTGGACACTGGACGGG

Phenotype

MIM: 603801 MIM: 606116

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

ACBD7 PubMed Links

Additional Information

For this assay, SNP(s) [rs7896053] 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	464	Missense Mutation	ACC,TCC	T64S	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	464	Intron			NP_001091059.1
NM_001265601.1	464	Intron			NP_001252530.1
NM_006414.4	464	Intron			NP_006405.2
NM_183005.4	464	Intron			NP_892117.1
XM_006717363.1	464	Intron			XP_006717426.1
XM_006717364.3	464	Intron			XP_006717427.1
XM_011519293.1	464	Intron			XP_011517595.1
XM_017015479.1	464	Intron			XP_016870968.1
XM_017015480.1	464	Intron			XP_016870969.1
XM_017015481.1	464	Intron			XP_016870970.1

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