Product Details

SNP ID
rs137852932
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:130159982 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCGCGAGCGGCCTCGGGGACCAT[A/G]GGGAGCGATCGGGCCCGCAAGGGCG
Phenotype
MIM: 606797
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
ST14 PubMed Links

Gene Details

Gene
ST14
Gene Name
suppression of tumorigenicity 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021978.3 196 Missense Mutation ATA,ATG I1M NP_068813.1

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