Product Details
- SNP ID
-
hCV89104296
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:36276192 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CATGCGGCTGATGCTGTCTGAGGAG[C/G]TTTTGATATCCACTCTCCAGTCCAG
- Phenotype
-
MIM: 612299
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
COMMD9
PubMed Links
Gene Details
- Gene
- COMMD9
- Gene Name
- COMM domain containing 9
There are no transcripts associated with this gene.
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