Product Details

SNP ID: rs11614917
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:107776225 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATGAGAGGAACATTTTCTTGCATTC[C/T]TTCCTTCGGGAATTGTATTCAAAAT
Phenotype: MIM: 609155
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ASCL4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_203436.2	1841	UTR 3			NP_982260.2