Product Details

SNP ID
rs34716166
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:32235443 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTATCTGTGAGTCTCCAGTTTTTCA[A/G]CCCAAGCTTGACGAGTTGTGGGACC
Phenotype
MIM: 606831
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NLRC4 PubMed Links

Gene Details

Gene
NLRC4
Gene Name
NLR family CARD domain containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199138.1 2884 Silent Mutation CTG,TTG L914L NP_001186067.1
NM_001199139.1 2884 Silent Mutation CTG,TTG L914L NP_001186068.1
NM_001302504.1 2884 Silent Mutation CTG,TTG L249L NP_001289433.1
NM_021209.4 2884 Silent Mutation CTG,TTG L914L NP_067032.3
XM_017004619.1 2884 Intron XP_016860108.1

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