Product Details

SNP ID
rs144993105
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:50697303 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGAGGAAAGAGCAAGTGTCCTCCT[C/T]GGACATTCTCCGGGTAAGAGGAGCA
Phenotype
MIM: 605956
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NOD2 PubMed Links

Gene Details

Gene
NOD2
Gene Name
nucleotide binding oligomerization domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001293557.1 165 Intron NP_001280486.1
NM_022162.2 165 Silent Mutation CTC,CTT L20L NP_071445.1
XM_005256084.3 165 Intron XP_005256141.1
XM_006721242.3 165 Intron XP_006721305.1
XM_006721243.3 165 Intron XP_006721306.1
XM_011523259.2 165 Intron XP_011521561.1
XM_011523260.2 165 Intron XP_011521562.1
XM_011523261.1 165 Intron XP_011521563.1
XM_017023535.1 165 Intron XP_016879024.1
XM_017023536.1 165 Intron XP_016879025.1
XM_017023537.1 165 Intron XP_016879026.1
XM_017023538.1 165 Intron XP_016879027.1

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