Product Details

SNP ID: rs10040598
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:148986157 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TAGCCTATTTTACTGCCCGTGTGAA[A/C]TTGGGTATGTTACATAACTGCCTTA
Phenotype: MIM: 608206
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: SH3TC2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024577.3	22573	UTR 3			NP_078853.2