Product Details

SNP ID

rs12353537

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:130697777 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTGATGTAAATATGTGGCTTGTTC[A/G]ATTTCAGATTACTGGTTCATGTTTT

Phenotype

MIM: 602238

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

EXOSC2 PubMed Links

Gene Details

Gene

EXOSC2

Gene Name

exosome component 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282708.1	450	Intron			NP_001269637.1
NM_001282709.1	450	Intron			NP_001269638.1
NM_014285.6	450	Intron			NP_055100.2
XM_005272176.2	450	Intron			XP_005272233.1
XM_006717023.2	450	Intron			XP_006717086.1
XM_017014558.1	450	UTR 5			XP_016870047.1

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