Product Details

SNP ID
rs201930699
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:72816785 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACAAGTTCTCAAAGAAGCTGCAGC[C/T]GGAGCCAAACAGTGTCACTCCCACC
Phenotype
Polymorphism
C/T, 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_001318766.1 195 UTR 5 NP_001305695.1
NM_033388.1 195 Missense Mutation CCG,CTG P59L NP_203746.1
XM_005274376.4 195 Missense Mutation CCG,CTG P59L XP_005274433.1
XM_006718732.2 195 Missense Mutation CCG,CTG P59L XP_006718795.1
XM_006718733.3 195 Missense Mutation CCG,CTG P59L XP_006718796.1
XM_006718734.2 195 Intron XP_006718797.1
XM_011545332.1 195 Missense Mutation CCG,CTG P59L XP_011543634.1
XM_011545333.1 195 UTR 5 XP_011543635.1
XM_011545334.1 195 UTR 5 XP_011543636.1

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