Product Details

SNP ID: rs117029992
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:2268840 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCTCTGTGCCCTTAGAAAATCCTCT[C/T]CCCTCCGGAAAAATCTCCAAGTGTT
Phenotype: MIM: 601886
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ASCL2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005170.2	1507	UTR 3			NP_005161.1