Product Details

SNP ID
rs1802150
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:85614746 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATCAGTCTCCAATTTTACAGAGGC[C/T]CTACTGTTTCTACTTCCACTGTTGC
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 2274 Intron NP_001153145.1
NM_001159674.1 2274 Intron NP_001153146.1
NM_001159675.1 2274 UTR 3 NP_001153147.1
NM_001159676.1 2274 Intron NP_001153148.1
NM_001159677.1 2274 Intron NP_001153149.1
NM_001253771.1 2274 Intron NP_001240700.1
NM_006372.4 2274 UTR 3 NP_006363.4
XM_005248635.4 2274 Intron XP_005248692.1
XM_005248636.2 2274 UTR 3 XP_005248693.1
XM_005248637.2 2274 UTR 3 XP_005248694.1
XM_017010176.1 2274 Intron XP_016865665.1
XM_017010177.1 2274 Intron XP_016865666.1
XM_017010178.1 2274 Intron XP_016865667.1
XM_017010179.1 2274 Intron XP_016865668.1
XM_017010180.1 2274 Intron XP_016865669.1

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