Product Details

SNP ID
rs148680614
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:85614956 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGCGCTTTCCTCCTACATTTCCAC[A/C]GCGGCCACCCCTCGCACCACGTACC
Phenotype
MIM: 616686
Polymorphism
A/C, Transversion 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 2064 Intron NP_001153145.1
NM_001159674.1 2064 Intron NP_001153146.1
NM_001159675.1 2064 Missense Mutation GGT,TGT G523C NP_001153147.1
NM_001159676.1 2064 Intron NP_001153148.1
NM_001159677.1 2064 Intron NP_001153149.1
NM_001253771.1 2064 Intron NP_001240700.1
NM_006372.4 2064 Missense Mutation GGT,TGT G558C NP_006363.4
XM_005248635.4 2064 Intron XP_005248692.1
XM_005248636.2 2064 Missense Mutation GGT,TGT G460C XP_005248693.1
XM_005248637.2 2064 Missense Mutation GGT,TGT G558C XP_005248694.1
XM_017010176.1 2064 Missense Mutation GGT,TGT G558C XP_016865665.1
XM_017010177.1 2064 Missense Mutation GGT,TGT G558C XP_016865666.1
XM_017010178.1 2064 Intron XP_016865667.1
XM_017010179.1 2064 Intron XP_016865668.1
XM_017010180.1 2064 Intron XP_016865669.1

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