Product Details
- SNP ID
-
rs113191234
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
1
- Location
-
Chr.1:220880246 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CATCACCCGCAACAACAACAGCAGC[A/C]GCAACAGCCGCAGCAGCAACAGCCT
- Phenotype
-
MIM: 142995
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
HLX
PubMed Links
Gene Details
- Gene
- HLX
- Gene Name
- H2.0 like homeobox
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_021958.3 |
846 |
Missense Mutation |
CAG,CCG |
Q130P |
NP_068777.1 |
- Gene
- HLX-AS1
- Gene Name
- HLX antisense RNA 1
There are no transcripts associated with this gene.
View Full Product Details