Product Details
- SNP ID
-
rs200620036
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:77020558 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGTCATGCACCACCTGGGCTACCCC[A/G]TGCCCGGCCAGCTTGGCAACGTCGT
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FOXB2
PubMed Links
Gene Details
- Gene
- FOXB2
- Gene Name
- forkhead box B2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001013735.1 |
904 |
Missense Mutation |
ATG,GTG |
M302V |
NP_001013757.1 |
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