Product Details

SNP ID

rs62624971

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:122981641 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGTGGGCCTCTGAGAAGACGCCG[C/G]GTGTAGAGGAGAGGTGAAGTTGAGA

Phenotype

MIM: 611074

Polymorphism

C/G, 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	31	Missense Mutation	CCG,GCG	P11A	NP_001091639.1

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