Product Details
- SNP ID
-
rs201755479
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
8
- Location
-
Chr.1:220880356 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAACCCCCACCACAGTGGCTCTGCC[C/T]CGGCCCCCTCCAGCAAAGACCTCAA
- Phenotype
-
MIM: 142995
- Polymorphism
- C/T, Transition 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 |
956 |
Missense Mutation |
CCG,TCG |
P167S |
NP_068777.1 |
- Gene
- HLX-AS1
- Gene Name
- HLX antisense RNA 1
There are no transcripts associated with this gene.
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