Product Details

SNP ID: rs141105892
Assay Type: Functionally tested
NCBI dbSNP Submissions: 17
Location: Chr.1:15462779 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGGCTGGGCCGGCACAACCTCTAC[A/G]TTGCGGAGTCCGGCTCGCTGGCAGT
Phenotype: MIM: 609443
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CELA2A PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033440.2	300	Missense Mutation	ATT,GTT	I92V	NP_254275.1