Product Details

SNP ID
rs183029490
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:57436682 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCACCCTCGTCCTCATCGGGCTC[A/G]CAGGTGGCCACGTCGGGCCAGCTGG
Phenotype
MIM: 604894
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ONECUT2 PubMed Links

Gene Details

Gene
ONECUT2
Gene Name
one cut homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004852.2 1263 Silent Mutation TCA,TCG S322S NP_004843.2
XM_017026096.1 1263 Silent Mutation TCA,TCG S322S XP_016881585.1

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