Product Details

SNP ID
rs11671248
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:55785653 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGGGGTTGCCTAGATGCTGTATTT[A/G]ACGTTCTCATGGCTGCAGACATTCT
Phenotype
MIM: 609664
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NLRP11 PubMed Links

Gene Details

Gene
NLRP11
Gene Name
NLR family pyrin domain containing 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297743.1 2935 Missense Mutation TCA,TTA S926L NP_001284672.1
NM_145007.3 2935 Missense Mutation TCA,TTA S1025L NP_659444.2

View Full Product Details