Product Details

SNP ID
rs144922246
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:38773307 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTGCCCAGAAAAGCCCACATTTAC[A/G]CCTATCCTTGGGCCATTCCAAGTAT
Phenotype
MIM: 606270
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TLR10 PubMed Links

Gene Details

Gene
TLR10
Gene Name
toll like receptor 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001017388.2 2416 Missense Mutation CGT,TGT R762C NP_001017388.1
NM_001195106.1 2416 Missense Mutation CGT,TGT R762C NP_001182035.1
NM_001195107.1 2416 Missense Mutation CGT,TGT R762C NP_001182036.1
NM_001195108.1 2416 Missense Mutation CGT,TGT R748C NP_001182037.1
NM_030956.3 2416 Missense Mutation CGT,TGT R762C NP_112218.2
XM_011513760.2 2416 Missense Mutation CGT,TGT R748C XP_011512062.1
XM_011513761.2 2416 Missense Mutation CGT,TGT R762C XP_011512063.1
XM_011513762.2 2416 Missense Mutation CGT,TGT R762C XP_011512064.1

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