Product Details

SNP ID
rs2618395
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:12004602 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCGGACAGCAGCTTCATCGCCAA[C/T]CTGCCCAACGGCTACATGACCGACC
Phenotype
MIM: 600755
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SYN2 PubMed Links

Gene Details

Gene
SYN2
Gene Name
synapsin II
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003178.5 243 Silent Mutation AAC,AAT N17N NP_003169.2
NM_133625.4 243 Silent Mutation AAC,AAT N17N NP_598328.1
XM_006713311.3 243 Silent Mutation AAC,AAT N17N XP_006713374.1
XM_006713312.3 243 Intron XP_006713375.1
XM_006713313.2 243 Intron XP_006713376.1
XM_017007087.1 243 Intron XP_016862576.1

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