Product Details

SNP ID
rs150828068
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:138596468 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGGAGAGTGAATGCAGAAATGGC[A/G]CATACAACACAGACAGATGAGAAGA
Phenotype
MIM: 611700
Polymorphism
A/G, 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 1107 Silent Mutation TGC,TGT C472C NP_001132928.1
NM_174959.3 1107 Silent Mutation TGC,TGT C320C NP_777619.1
XM_005250143.3 1107 Silent Mutation TGC,TGT C472C XP_005250200.1
XM_011515797.2 1107 Silent Mutation TGC,TGT C320C XP_011514099.1
XM_017011746.1 1107 Silent Mutation TGC,TGT C381C XP_016867235.1
XM_017011747.1 1107 Silent Mutation TGC,TGT C320C XP_016867236.1
XM_017011748.1 1107 Silent Mutation TGC,TGT C320C XP_016867237.1

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