Product Details

SNP ID
rs9344537
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:85608958 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTGTGAGCACTGCTTCATAATTA[A/G]CATCTTAAGAAAAGTAGTGGCATGC
Phenotype
MIM: 616686
Polymorphism
A/G, 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 5772 UTR 3 NP_001153145.1
NM_001159674.1 5772 UTR 3 NP_001153146.1
NM_001159675.1 5772 Intron NP_001153147.1
NM_001159676.1 5772 UTR 3 NP_001153148.1
NM_001159677.1 5772 UTR 3 NP_001153149.1
NM_001253771.1 5772 UTR 3 NP_001240700.1
NM_006372.4 5772 Intron NP_006363.4
XM_005248635.4 5772 UTR 3 XP_005248692.1
XM_005248636.2 5772 Intron XP_005248693.1
XM_005248637.2 5772 Intron XP_005248694.1
XM_017010176.1 5772 UTR 3 XP_016865665.1
XM_017010177.1 5772 UTR 3 XP_016865666.1
XM_017010178.1 5772 UTR 3 XP_016865667.1
XM_017010179.1 5772 UTR 3 XP_016865668.1
XM_017010180.1 5772 Intron XP_016865669.1

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