Product Details

SNP ID

rs141049984

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:7960011 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCTAAACAGGGAGAAATTCTGAAG[C/G]AGAACTTGAGCTCCAAGTTCGAGAA

Phenotype

MIM: 609662

Polymorphism

C/G, Transversion 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	1828	Missense Mutation	TCC,TGC	S534C	NP_789791.1
XM_011520043.2	1828	Missense Mutation	TCC,TGC	S534C	XP_011518345.1

View Full Product Details