Product Details

SNP ID

rs140212063

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:54101851 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGCGTCGGGAGCCAGGTGCACTAC[C/G]CGCGCTCCGAGGATGAGGACTCCCT

Phenotype

MIM: 616253

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

GSX2 PubMed Links

Gene Details

Gene

GSX2

Gene Name

GS homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_133267.2	1108	Missense Mutation	CCG,GCG	P282A	NP_573574.1

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