rs11074945

Positions:

• chr16-11012201-G-A

Variant summary

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

The NM_015226.3(CLEC16A):​c.1304-7992G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0565 in 152,216 control chromosomes in the GnomAD database, including 364 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 0.057 (364 hom., cov: 32)
• Consequence: CLEC16A NM_015226.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.504

Genes affected

CLEC16A (HGNC:29013): (C-type lectin domain containing 16A) This gene encodes a member of the C-type lectin domain containing family. Single nucleotide polymorphisms in introns of this gene have been associated with diabetes mellitus, multiple sclerosis and rheumatoid arthritis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]

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 (NFE) allele frequency at 95% confidence interval = 0.084 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CLEC16A	NM_015226.3	c.1304-7992G>A		intron_variant		ENST00000409790.6	NP_056041.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CLEC16A	ENST00000409790.6	c.1304-7992G>A		intron_variant		5	NM_015226.3	ENSP00000387122	A1
CLEC16A	ENST00000409552.4	c.1250-7992G>A		intron_variant		1		ENSP00000386495
CLEC16A	ENST00000703130.1	c.1298-7992G>A		intron_variant				ENSP00000515187	P4
CLEC16A	ENST00000494853.1	n.779-7992G>A		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.0566 AC: 8610 AN: 152098 Hom.: 364 Cov.: 32

Gnomad AFR AF: 0.0137

Gnomad AMI AF: 0.0373

Gnomad AMR AF: 0.0431

Gnomad ASJ AF: 0.0473

Gnomad EAS AF: 0.00115

Gnomad SAS AF: 0.0815

Gnomad FIN AF: 0.0781

Gnomad MID AF: 0.0633

Gnomad NFE AF: 0.0858

Gnomad OTH AF: 0.0493

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.0565 AC: 8605 AN: 152216 Hom.: 364 Cov.: 32 AF XY: 0.0562 AC XY: 4180 AN XY: 74416

Gnomad4 AFR AF: 0.0137

Gnomad4 AMR AF: 0.0431

Gnomad4 ASJ AF: 0.0473

Gnomad4 EAS AF: 0.00116

Gnomad4 SAS AF: 0.0812

Gnomad4 FIN AF: 0.0781

Gnomad4 NFE AF: 0.0858

Gnomad4 OTH AF: 0.0488

Alfa AF: 0.0818 Hom.: 364

Bravo AF: 0.0503

Asia WGS AF: 0.0310 AC: 109 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	1.2
DANN	Benign	0.59

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: rs11074945; hg19: chr16-11106058;