Product Details

SNP ID
rs16990599
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32511251 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCAGGAGGATGAAGCAAAGTTCTAC[C/T]GGATTATAAATGGTCTGATCTATTC
Phenotype
MIM: 602705
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SYN3 PubMed Links

Gene Details

Gene
SYN3
Gene Name
synapsin III
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135774.1 4852 Intron NP_001129246.1
NM_003490.3 4852 Intron NP_003481.3
NM_133633.2 4852 Intron NP_598344.2
XM_011530405.2 4852 UTR 3 XP_011528707.1
XM_011530406.2 4852 UTR 3 XP_011528708.1
XM_011530407.2 4852 UTR 3 XP_011528709.1
XM_011530408.1 4852 UTR 3 XP_011528710.1
XM_011530410.2 4852 UTR 3 XP_011528712.1
XM_017028960.1 4852 UTR 3 XP_016884449.1
XM_017028961.1 4852 UTR 3 XP_016884450.1
XM_017028962.1 4852 UTR 3 XP_016884451.1
XM_017028963.1 4852 UTR 3 XP_016884452.1
XM_017028964.1 4852 UTR 3 XP_016884453.1
XM_017028965.1 4852 UTR 3 XP_016884454.1

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