Product Details

SNP ID

rs139911906

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:37780719 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTGGAGAAGATCTGTTTTCTTTGA[G/T]CTGACGTCATGTGTTCACAAGCTTC

Phenotype

MIM: 606489

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

EXOSC3 PubMed Links

Additional Information

For this assay, SNP(s) [rs1059059] 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

EXOSC3

Gene Name

exosome component 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002269.2	836	UTR 3			NP_001002269.1
NM_016042.3	836	Missense Mutation			NP_057126.2

Gene

LOC105376037

Gene Name

uncharacterized LOC105376037

There are no transcripts associated with this gene.

Gene

TRMT10B

Gene Name

tRNA methyltransferase 10B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286950.1	836	Intron			NP_001273879.1
NM_001286951.1	836	Intron			NP_001273880.1
NM_001286952.1	836	Intron			NP_001273881.1
NM_001286953.1	836	Intron			NP_001273882.1
NM_001286954.1	836	Intron			NP_001273883.1
NM_144964.3	836	Intron			NP_659401.2
XM_005251375.2	836	Intron			XP_005251432.1
XM_005251379.2	836	Intron			XP_005251436.1
XM_011517735.2	836	Intron			XP_011516037.1
XM_011517736.2	836	Intron			XP_011516038.1
XM_011517738.2	836	Intron			XP_011516040.1
XM_011517739.2	836	Intron			XP_011516041.1
XM_011517742.1	836	Intron			XP_011516044.1
XM_011517743.2	836	Intron			XP_011516045.1
XM_017014313.1	836	Intron			XP_016869802.1

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