Product Details

SNP ID: rs9782
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.12:102958048 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CAGGGAGGAGAAAAAGCATTTTCAC[C/T]TTTTTTGCTCCCACTCTAAGAAGTC
Phenotype: MIM: 100790
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ASCL1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004316.3	375	UTR 5			NP_004307.2