Product Details

SNP ID

rs140992190

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:7960240 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGCGGAAGCTGTAGAACTTCTTGA[C/T]GGCAAGTCCCAATTGGTAGTCGTTA

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	1599	Missense Mutation	ATC,GTC	I458V	NP_789791.1
XM_011520043.2	1599	Missense Mutation	ATC,GTC	I458V	XP_011518345.1

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