Product Details

SNP ID

rs150443652

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:55896079 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTACTGCTGCTGAGAACAGAGAAGA[A/G]ATGCTGGCAGCAAGCAGTTGTCAGA

Phenotype

MIM: 609660

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NLRP13 PubMed Links

Gene Details

Gene

NLRP13

Gene Name

NLR family pyrin domain containing 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321057.1	3023	Missense Mutation	CTC,TTC	L1000F	NP_001307986.1
NM_176810.2	3023	Missense Mutation	CTC,TTC	L1000F	NP_789780.2

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