Product Details

SNP ID

rs77880799

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:77637015 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGGTTCGGGCCGCCCTGGGGCC[C/G]GGGCTGCTTGTCCGGGTCTTTGGCG

Phenotype

MIM: 604529

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

OTP PubMed Links

Gene Details

Gene

OTP

Gene Name

orthopedia homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032109.2	401	Missense Mutation	CGG,GGG	R85G	NP_115485.1

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