Product Details

SNP ID

rs145905387

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:33027077 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCATCCTGGGGACAAGCTAGGAG[G/T]CAGTGGCTTCAAGTCATCCTCGTCC

Phenotype

MIM: 606386

Polymorphism

G/T, Transversion 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	603	Missense Mutation	GGC,GTC	G72V	NP_005797.1
XM_005260908.1	603	Missense Mutation	GGC,GTC	G72V	XP_005260965.1

View Full Product Details