Product Details

SNP ID
rs113377061
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:233251887 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGGAAGCGCCACATCTCGGAGCA[A/G]CTGAGGCGCCGGGACCGGCTGCAGA
Phenotype
MIM: 610767
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ATG16L1 PubMed Links

Gene Details

Gene
ATG16L1
Gene Name
autophagy related 16 like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001190266.1 254 UTR 5 NP_001177195.1
NM_001190267.1 254 UTR 5 NP_001177196.1
NM_017974.3 254 Silent Mutation CAA,CAG Q20Q NP_060444.3
NM_030803.6 254 Silent Mutation CAA,CAG Q20Q NP_110430.5
NM_198890.2 254 Silent Mutation CAA,CAG Q20Q NP_942593.2
XM_005246082.2 254 Silent Mutation CAA,CAG Q20Q XP_005246139.1
XM_005246084.2 254 Silent Mutation CAA,CAG Q20Q XP_005246141.1
XM_005246086.2 254 Silent Mutation CAA,CAG Q20Q XP_005246143.1
XM_006712608.2 254 Silent Mutation CAA,CAG Q20Q XP_006712671.1

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