Product Details

SNP ID
rs8139438
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32509153 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATTTAACCAAAGTACGGTACCATTT[C/T]ATCGCGCTGACGGGAGGAAGATCTG
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 6950 Intron NP_001129246.1
NM_003490.3 6950 Intron NP_003481.3
NM_133633.2 6950 Intron NP_598344.2
XM_011530405.2 6950 UTR 3 XP_011528707.1
XM_011530406.2 6950 UTR 3 XP_011528708.1
XM_011530407.2 6950 UTR 3 XP_011528709.1
XM_011530408.1 6950 UTR 3 XP_011528710.1
XM_011530410.2 6950 UTR 3 XP_011528712.1
XM_017028960.1 6950 UTR 3 XP_016884449.1
XM_017028961.1 6950 UTR 3 XP_016884450.1
XM_017028962.1 6950 UTR 3 XP_016884451.1
XM_017028963.1 6950 UTR 3 XP_016884452.1
XM_017028964.1 6950 UTR 3 XP_016884453.1
XM_017028965.1 6950 UTR 3 XP_016884454.1

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