Product Details

SNP ID
rs199985220
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:138596516 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAGACACAGGGCCCCCAGTATTGA[C/T]GCACTCATAAGAACCTGCAAGTCAC
Phenotype
MIM: 611700
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SVOPL PubMed Links

Gene Details

Gene
SVOPL
Gene Name
SVOP like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001139456.1 1059 Silent Mutation GCA,GCG A456A NP_001132928.1
NM_174959.3 1059 Silent Mutation GCA,GCG A304A NP_777619.1
XM_005250143.3 1059 Silent Mutation GCA,GCG A456A XP_005250200.1
XM_011515797.2 1059 Silent Mutation GCA,GCG A304A XP_011514099.1
XM_017011746.1 1059 Silent Mutation GCA,GCG A365A XP_016867235.1
XM_017011747.1 1059 Silent Mutation GCA,GCG A304A XP_016867236.1
XM_017011748.1 1059 Silent Mutation GCA,GCG A304A XP_016867237.1

View Full Product Details