Product Details

SNP ID
rs144710636
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:54041070 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGCTCAGCATAGGTCACTCCTTGG[G/T]GGTCTGCCGTCTTTGGAGAAAATAG
Phenotype
MIM: 616804
Polymorphism
G/T, Transversion 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 1085 Missense Mutation NP_001275720.1
NM_001288792.1 1085 Missense Mutation NP_001275721.1
NM_001288793.1 1085 Missense Mutation NP_001275722.1
NM_198481.3 1085 Missense Mutation NP_940883.2
XM_011526845.1 1085 Missense Mutation XP_011525147.1
XM_011526846.1 1085 Missense Mutation XP_011525148.1
XM_011526847.1 1085 Missense Mutation XP_011525149.1
XM_011526848.1 1085 Missense Mutation XP_011525150.1
XM_011526849.1 1085 Missense Mutation XP_011525151.1
XM_017026666.1 1085 Intron XP_016882155.1

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