Product Details

SNP ID

rs13357072

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:77630753 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCGCACGGAACACGTTGGTCGTCTT[C/T]TTGCGCTTCTTCCACTTGGCGCGTC

Phenotype

MIM: 604529

Polymorphism

C/T, Transition 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	637	Silent Mutation	AAA,AAG	K163K	NP_115485.1

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