Product Details

SNP ID
rs117793750
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:85610380 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCACTTGATGTGTATATATTTCA[C/T]CACCACTGTTTACATTACCCTTCTT
Phenotype
MIM: 616686
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SYNCRIP PubMed Links

Gene Details

Gene
SYNCRIP
Gene Name
synaptotagmin binding cytoplasmic RNA interacting protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001159673.1 4350 UTR 3 NP_001153145.1
NM_001159674.1 4350 UTR 3 NP_001153146.1
NM_001159675.1 4350 Intron NP_001153147.1
NM_001159676.1 4350 UTR 3 NP_001153148.1
NM_001159677.1 4350 UTR 3 NP_001153149.1
NM_001253771.1 4350 UTR 3 NP_001240700.1
NM_006372.4 4350 Intron NP_006363.4
XM_005248635.4 4350 UTR 3 XP_005248692.1
XM_005248636.2 4350 Intron XP_005248693.1
XM_005248637.2 4350 Intron XP_005248694.1
XM_017010176.1 4350 UTR 3 XP_016865665.1
XM_017010177.1 4350 UTR 3 XP_016865666.1
XM_017010178.1 4350 UTR 3 XP_016865667.1
XM_017010179.1 4350 UTR 3 XP_016865668.1
XM_017010180.1 4350 Intron XP_016865669.1

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