Product Details

SNP ID
rs35124349
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:32933289 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAGGCCATTCTGGAGAATGAAGAC[C/T]GGATCGAAGATGCCTCGTAAGGCCA
Phenotype
MIM: 615949
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM98 PubMed Links

Gene Details

Gene
TMEM98
Gene Name
transmembrane protein 98
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001033504.1 629 Missense Mutation CGG,TGG R83W NP_001028676.1
NM_001301746.1 629 Missense Mutation CGG,TGG R83W NP_001288675.1
NM_015544.2 629 Missense Mutation CGG,TGG R83W NP_056359.2

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