Product Details

SNP ID
rs201700689
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:72821689 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGATGGCCTACCAGGTGGTGGAG[A/G]AGGGCGCGGCCCTGGGCACGCTGGA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ATG16L2 PubMed Links

Gene Details

Gene
ATG16L2
Gene Name
autophagy related 16 like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318766.1 828 Missense Mutation AAG,GAG K8E NP_001305695.1
NM_033388.1 828 Missense Mutation AAG,GAG K114E NP_203746.1
XM_005274376.4 828 Missense Mutation AAG,GAG K114E XP_005274433.1
XM_006718732.2 828 Missense Mutation AAG,GAG K114E XP_006718795.1
XM_006718733.3 828 Missense Mutation AAG,GAG K114E XP_006718796.1
XM_006718734.2 828 Intron XP_006718797.1
XM_011545332.1 828 Missense Mutation AAG,GAG K114E XP_011543634.1
XM_011545333.1 828 Missense Mutation AAG,GAG K8E XP_011543635.1
XM_011545334.1 828 Missense Mutation AAG,GAG K8E XP_011543636.1

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