rs2289476

Positions:

• chr2-233272910-C-A
• chr2-233272910-C-G
• chr2-233272910-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_030803.7(ATG16L1):​c.708-56C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0715 in 1,478,832 control chromosomes in the GnomAD database, including 4,823 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.097 (927 hom., cov: 33)
  • Exomes 𝑓: 0.069 (3896 hom.)
• Consequence: ATG16L1 NM_030803.7 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.107

Genes affected

ATG16L1 (HGNC:21498): (autophagy related 16 like 1) The protein encoded by this gene is part of a large protein complex that is necessary for autophagy, the major process by which intracellular components are targeted to lysosomes for degradation. Defects in this gene are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.169 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ATG16L1	NM_030803.7	c.708-56C>A		intron_variant		ENST00000392017.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ATG16L1	ENST00000392017.9	c.708-56C>A		intron_variant		1	NM_030803.7	P3

Frequencies

GnomAD3 genomes AF: 0.0966 AC: 14685 AN: 152082 Hom.: 926 Cov.: 33

Gnomad AFR AF: 0.172

Gnomad AMI AF: 0.0417

Gnomad AMR AF: 0.0799

Gnomad ASJ AF: 0.0784

Gnomad EAS AF: 0.0424

Gnomad SAS AF: 0.154

Gnomad FIN AF: 0.0818

Gnomad MID AF: 0.0538

Gnomad NFE AF: 0.0591

Gnomad OTH AF: 0.0845

GnomAD4 exome AF: 0.0686 AC: 91047 AN: 1326632 Hom.: 3896 AF XY: 0.0710 AC XY: 47374 AN XY: 667552

Gnomad4 AFR exome AF: 0.174

Gnomad4 AMR exome AF: 0.0591

Gnomad4 ASJ exome AF: 0.0741

Gnomad4 EAS exome AF: 0.0429

Gnomad4 SAS exome AF: 0.153

Gnomad4 FIN exome AF: 0.0772

Gnomad4 NFE exome AF: 0.0588

Gnomad4 OTH exome AF: 0.0768

GnomAD4 genome AF: 0.0966 AC: 14706 AN: 152200 Hom.: 927 Cov.: 33 AF XY: 0.0987 AC XY: 7346 AN XY: 74408

Gnomad4 AFR AF: 0.172

Gnomad4 AMR AF: 0.0796

Gnomad4 ASJ AF: 0.0784

Gnomad4 EAS AF: 0.0429

Gnomad4 SAS AF: 0.153

Gnomad4 FIN AF: 0.0818

Gnomad4 NFE AF: 0.0591

Gnomad4 OTH AF: 0.0879

Alfa AF: 0.0615 Hom.: 211

Bravo AF: 0.0977

Asia WGS AF: 0.123 AC: 430 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.58
DANN	Benign	0.67

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs2289476; hg19: chr2-234181556;