Product Details

SNP ID
rs1894450
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32511734 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCAGGCCTGAGCCTACCAGTCTCCA[C/G]CTGCCAAATTATGGCTCCCAATAGT
Phenotype
MIM: 602705
Polymorphism
C/G, Transversion 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 4369 Intron NP_001129246.1
NM_003490.3 4369 Intron NP_003481.3
NM_133633.2 4369 Intron NP_598344.2
XM_011530405.2 4369 UTR 3 XP_011528707.1
XM_011530406.2 4369 UTR 3 XP_011528708.1
XM_011530407.2 4369 UTR 3 XP_011528709.1
XM_011530408.1 4369 UTR 3 XP_011528710.1
XM_011530410.2 4369 UTR 3 XP_011528712.1
XM_017028960.1 4369 UTR 3 XP_016884449.1
XM_017028961.1 4369 UTR 3 XP_016884450.1
XM_017028962.1 4369 UTR 3 XP_016884451.1
XM_017028963.1 4369 UTR 3 XP_016884452.1
XM_017028964.1 4369 UTR 3 XP_016884453.1
XM_017028965.1 4369 UTR 3 XP_016884454.1

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