Product Details

SNP ID
rs202035279
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:54041917 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTAAACTTCCCCTGTCCCTTACC[A/G]GCAGCCTCCTGCTCCGGAAGTTTGG
Phenotype
MIM: 616804
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
VSTM1 PubMed Links

Gene Details

Gene
VSTM1
Gene Name
V-set and transmembrane domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001288791.1 1035 Silent Mutation GCC,GCT A96A NP_001275720.1
NM_001288792.1 1035 Silent Mutation GCC,GCT A153A NP_001275721.1
NM_001288793.1 1035 Silent Mutation GCC,GCT A64A NP_001275722.1
NM_198481.3 1035 Silent Mutation GCC,GCT A184A NP_940883.2
XM_011526845.1 1035 Silent Mutation GCC,GCT A312A XP_011525147.1
XM_011526846.1 1035 Silent Mutation GCC,GCT A282A XP_011525148.1
XM_011526847.1 1035 Missense Mutation CCG,CTG P305L XP_011525149.1
XM_011526848.1 1035 Silent Mutation GCC,GCT A251A XP_011525150.1
XM_011526849.1 1035 Silent Mutation GCC,GCT A214A XP_011525151.1
XM_017026666.1 1035 UTR 3 XP_016882155.1

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