Product Details

SNP ID: rs9611424
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:40830659 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AAATAAAAGCTCACTGAATAATTTA[A/C]GACTAAAAATGTCCCCCAAATTAGA
Phenotype: MIM: 606796
Polymorphism: A/C, Transversion 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		Intron			NP_001265518.1
NM_003932.4		Intron			NP_003923.2