Product Details

SNP ID

rs11685932

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:233257676 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTGAAATCAAATTAGCAGATTGCA[A/G]TAAGCTCTTATTTTTCTTTAAGAAC

Phenotype

MIM: 610767

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ATG16L1 PubMed Links

Gene Details

Gene

ATG16L1

Gene Name

autophagy related 16 like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190266.1		Intron			NP_001177195.1
NM_001190267.1		Intron			NP_001177196.1
NM_017974.3		Intron			NP_060444.3
NM_030803.6		Intron			NP_110430.5
NM_198890.2		Intron			NP_942593.2
XM_005246082.2		Intron			XP_005246139.1
XM_005246084.2		Intron			XP_005246141.1
XM_005246086.2		Intron			XP_005246143.1
XM_006712608.2		Intron			XP_006712671.1

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