Product Details

SNP ID
rs137920368
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:7959718 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTAGAAGCTTCCTTTTGTGTTCCTG[C/T]TATATTATCTTTGCCCTCCTTCTGT
Phenotype
MIM: 609662
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
NLRP10 PubMed Links

Gene Details

Gene
NLRP10
Gene Name
NLR family pyrin domain containing 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_176821.3 2121 Missense Mutation ACA,GCA T632A NP_789791.1
XM_011520043.2 2121 Missense Mutation ACA,GCA T632A XP_011518345.1

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