Product Details
- SNP ID
-
rs148166215
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:77637029 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCCTGGGGCCCGGGCTGCTTGTCC[G/T]GGTCTTTGGCGCTCACCGCCAGCGA
- Phenotype
-
MIM: 604529
- Polymorphism
- G/T, 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 |
387 |
Missense Mutation |
|
|
NP_115485.1 |
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