Product Details

SNP ID

rs10751215

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.11:72815042 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GGCTGTGCATCTCAGGCTCTGCCGC[C/T]GACAGGCGACGCTGGCACAGGCTTA

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		Intron			NP_001305695.1
NM_033388.1		Intron			NP_203746.1
XM_005274376.4		Intron			XP_005274433.1
XM_006718732.2		Intron			XP_006718795.1
XM_006718733.3		Intron			XP_006718796.1
XM_006718734.2		Intron			XP_006718797.1
XM_011545332.1		Intron			XP_011543634.1
XM_011545333.1		Intron			XP_011543635.1
XM_011545334.1		Intron			XP_011543636.1

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