Product Details

SNP ID
rs202199122
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:45218249 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGGCCAGGGCCTGGGCACCCAGC[A/G]TGCCCACGATGCCATCCAGGGCCTC
Phenotype
MIM: 616927
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
EXOC3L2 PubMed Links

Gene Details

Gene
EXOC3L2
Gene Name
exocyst complex component 3 like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138568.3 652 Missense Mutation ACG,ATG T204M NP_612635.3

View Full Product Details