Product Details

SNP ID
rs148037199
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:173317879 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGATATCAGAATACTCAGACTGTT[C/T]GTCTTCCCACTCGCTGCTTCCGGAA
Phenotype
MIM: 603665
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
STC2 PubMed Links

Gene Details

Gene
STC2
Gene Name
stanniocalcin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003714.2 2187 Missense Mutation AAA,GAA K293E NP_003705.1

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