Product Details

SNP ID
rs139969359
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:72840931 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGTATGCCTTGATGCCTGTGAGAA[G/T]CCTGGTGACTCAGCATGAAGGCTTT
Phenotype
Polymorphism
G/T, Transversion 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 2306 Intron NP_001305695.1
NM_033388.1 2306 Intron NP_203746.1
XM_005274376.4 2306 Intron XP_005274433.1
XM_006718732.2 2306 Intron XP_006718795.1
XM_006718733.3 2306 Intron XP_006718796.1
XM_006718734.2 2306 Intron XP_006718797.1
XM_011545332.1 2306 Intron XP_011543634.1
XM_011545333.1 2306 Intron XP_011543635.1
XM_011545334.1 2306 Intron XP_011543636.1
Gene
FCHSD2
Gene Name
FCH and double SH3 domains 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014824.2 2306 Silent Mutation GGA,GGC G695G NP_055639.2
XM_011545409.1 2306 Silent Mutation GGA,GGC G674G XP_011543711.1
XM_011545410.2 2306 Silent Mutation GGA,GGC G670G XP_011543712.1
XM_017018632.1 2306 Silent Mutation GGA,GGC G674G XP_016874121.1

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