Product Details

SNP ID

rs17854475

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:33027310 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCGGTGCGCAAGCTTTCCAAGATC[A/G]CCACGCTGCTGCTGGCGCGCAACTA

Phenotype

MIM: 606386

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

OLIG2 PubMed Links

Gene Details

Gene

OLIG2

Gene Name

oligodendrocyte lineage transcription factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005806.3	836	Missense Mutation	ACC,GCC	T150A	NP_005797.1
XM_005260908.1	836	Missense Mutation	ACC,GCC	T150A	XP_005260965.1

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