Product Details

SNP ID
rs149771368
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:85610032 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGCATTTCCATTTCTCATATCCCA[A/T]GACATTCCATATAAATTGCATTATT
Phenotype
MIM: 616686
Polymorphism
A/T, 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 4698 UTR 3 NP_001153145.1
NM_001159674.1 4698 UTR 3 NP_001153146.1
NM_001159675.1 4698 Intron NP_001153147.1
NM_001159676.1 4698 UTR 3 NP_001153148.1
NM_001159677.1 4698 UTR 3 NP_001153149.1
NM_001253771.1 4698 UTR 3 NP_001240700.1
NM_006372.4 4698 Intron NP_006363.4
XM_005248635.4 4698 UTR 3 XP_005248692.1
XM_005248636.2 4698 Intron XP_005248693.1
XM_005248637.2 4698 Intron XP_005248694.1
XM_017010176.1 4698 UTR 3 XP_016865665.1
XM_017010177.1 4698 UTR 3 XP_016865666.1
XM_017010178.1 4698 UTR 3 XP_016865667.1
XM_017010179.1 4698 UTR 3 XP_016865668.1
XM_017010180.1 4698 Intron XP_016865669.1

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