Product Details

SNP ID
rs4257479
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:32512304 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGTGGACAGCAAAAGGAAGACAT[A/G]TCTCATGTTGCGAAGTGGGAGGCAA
Phenotype
MIM: 602705
Polymorphism
A/G, 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 3799 Intron NP_001129246.1
NM_003490.3 3799 Intron NP_003481.3
NM_133633.2 3799 Intron NP_598344.2
XM_011530405.2 3799 UTR 3 XP_011528707.1
XM_011530406.2 3799 UTR 3 XP_011528708.1
XM_011530407.2 3799 UTR 3 XP_011528709.1
XM_011530408.1 3799 UTR 3 XP_011528710.1
XM_011530410.2 3799 UTR 3 XP_011528712.1
XM_017028960.1 3799 UTR 3 XP_016884449.1
XM_017028961.1 3799 UTR 3 XP_016884450.1
XM_017028962.1 3799 UTR 3 XP_016884451.1
XM_017028963.1 3799 UTR 3 XP_016884452.1
XM_017028964.1 3799 UTR 3 XP_016884453.1
XM_017028965.1 3799 UTR 3 XP_016884454.1

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