Product Details

SNP ID
rs114793717
Assay Type
Functionally tested
NCBI dbSNP Submissions
16
Location
Chr.1:85163712 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGACCCCGGGGCCAAGCACGGTTA[C/G]TAGTGTGCTCTACACTAAACACCAA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SYDE2 PubMed Links

Gene Details

Gene
SYDE2
Gene Name
synapse defective Rho GTPase homolog 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032184.1 Intron NP_115560.1
XM_005271254.3 Intron XP_005271311.1
XM_006710946.3 Intron XP_006711009.1
XM_017002483.1 Intron XP_016857972.1
XM_017002484.1 Intron XP_016857973.1
XM_017002485.1 Intron XP_016857974.1
XM_017002486.1 Intron XP_016857975.1

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