Product Details
- SNP ID
-
rs199766120
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:53939455 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCCCAGCTTCGCCAGCTCCTACCA[C/G]GCGATGCCCGGCTACCTGGACGTGT
- Phenotype
-
MIM: 142976
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
HOXC13
PubMed Links
Gene Details
- Gene
- HOXC13
- Gene Name
- homeobox C13
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_017410.2 |
664 |
Missense Mutation |
CAC,CAG |
H183Q |
NP_059106.2 |
- Gene
- HOXC13-AS
- Gene Name
- HOXC13 antisense RNA
There are no transcripts associated with this gene.
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