Product Details

SNP ID

rs61737277

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:122977658 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCCAGCCTGGCGGCTCAGAGCAC[G/T]TGCGGCCCTGAGCCCAGCTCCCCCT

Phenotype

MIM: 611074

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

BSX PubMed Links

Gene Details

Gene

BSX

Gene Name

brain specific homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098169.1	693	Missense Mutation	CAA,CAC	Q231H	NP_001091639.1

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