Product Details

SNP ID
rs2618390
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:12006354 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGGCACATGGAAGAGGGTAATGGG[A/G]AAAGTGTAATGCATATGATAGTGCC
Phenotype
MIM: 600755
Polymorphism
A/G, 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 Intron NP_003169.2
NM_133625.4 Intron NP_598328.1
XM_006713311.3 Intron XP_006713374.1
XM_006713312.3 Intron XP_006713375.1
XM_006713313.2 Intron XP_006713376.1
XM_017007087.1 Intron XP_016862576.1

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