Product Details

SNP ID
rs12750669
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:109466875 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGACCGAGAGCGCCGGCCGCACGG[A/C]GGACAAGTCGCCGCGCCAGCAGGTA
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SYPL2 PubMed Links

Gene Details

Gene
SYPL2
Gene Name
synaptophysin like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040709.1 398 Missense Mutation GAG,GCG E11A NP_001035799.1
XM_011541283.2 398 Missense Mutation GAG,GCG E11A XP_011539585.1
XM_011541284.2 398 Missense Mutation GAG,GCG E11A XP_011539586.1
XM_011541285.1 398 Missense Mutation GAG,GCG E11A XP_011539587.1

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