Product Details

SNP ID
rs61894256
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:72837464 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGCAAATTTGATTTCTTAACCAA[A/G]GAAAAAAAAAAAAAACAAACCACAA
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 3771 Intron NP_001305695.1
NM_033388.1 3771 Intron NP_203746.1
XM_005274376.4 3771 Intron XP_005274433.1
XM_006718732.2 3771 Intron XP_006718795.1
XM_006718733.3 3771 Intron XP_006718796.1
XM_006718734.2 3771 Intron XP_006718797.1
XM_011545332.1 3771 Intron XP_011543634.1
XM_011545333.1 3771 Intron XP_011543635.1
XM_011545334.1 3771 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 3771 UTR 3 NP_055639.2
XM_011545409.1 3771 UTR 3 XP_011543711.1
XM_011545410.2 3771 UTR 3 XP_011543712.1
XM_017018632.1 3771 UTR 3 XP_016874121.1

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