Product Details
- SNP ID
-
rs138776675
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:56594291 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTGGTGGTCCTGGGGCTGCGGGCGA[C/T]ACCGGCCGGCGGCCAGCACTATCTC
- Phenotype
-
MIM: 602991
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NOG
PubMed Links
Gene Details
- Gene
- NOG
- Gene Name
- noggin
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_005450.4 |
593 |
Missense Mutation |
ACA,ATA |
T23I |
NP_005441.1 |
View Full Product Details