Product Details

SNP ID: rs200736981
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:40832642 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAATTTACAGGCAAGGGCAAGATCA[C/T]GGGCTGCTTCTTCCCAGTGGCCTAG
Phenotype: MIM: 606796
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ST13 PubMed Links

Gene Details

Gene: ST13
Gene Name: suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001278589.1	1076	Missense Mutation	CAT,CGT	H193R	NP_001265518.1
NM_003932.4	1076	Missense Mutation	CAT,CGT	H203R	NP_003923.2