chr16-11114037-T-C

Variant names:

• chr16-11114037-T-C
• rs9746695
• NM_015226.3:c.2117-6578T>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_015226.3(CLEC16A):​c.2117-6578T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.321 in 152,054 control chromosomes in the GnomAD database, including 7,877 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 0.32 (7877 hom., cov: 32)
• Consequence: CLEC16A NM_015226.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.296
• Publications: 20 publications found

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]

CLEC16A Gene-Disease associations (from GenCC):

• schizophrenia

  Inheritance: Unknown Classification: NO_KNOWN Submitted by: Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.379 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_015226.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CLEC16A	NM_015226.3	MANE Select	c.2117-6578T>C		intron	N/A	NP_056041.1
	CLEC16A	NM_001410905.1		c.2111-6578T>C		intron	N/A	NP_001397834.1
	CLEC16A	NM_001243403.2		c.2063-6578T>C		intron	N/A	NP_001230332.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CLEC16A	ENST00000409790.6	TSL:5 MANE Select	c.2117-6578T>C		intron	N/A	ENSP00000387122.1
	CLEC16A	ENST00000409552.4	TSL:1	c.2063-6578T>C		intron	N/A	ENSP00000386495.3
	CLEC16A	ENST00000703130.1		c.2111-6578T>C		intron	N/A	ENSP00000515187.1

Frequencies

GnomAD3 genomes AF: 0.321 AC: 48770 AN: 151936 Hom.: 7844 Cov.: 32

Gnomad AFR AF: 0.327

Gnomad AMI AF: 0.229

Gnomad AMR AF: 0.273

Gnomad ASJ AF: 0.419

Gnomad EAS AF: 0.230

Gnomad SAS AF: 0.392

Gnomad FIN AF: 0.313

Gnomad MID AF: 0.364

Gnomad NFE AF: 0.327

Gnomad OTH AF: 0.325

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

GnomAD4 genome AF: 0.321 AC: 48853 AN: 152054 Hom.: 7877 Cov.: 32 AF XY: 0.320 AC XY: 23746 AN XY: 74308

African (AFR) AF: 0.327 AC: 13573 AN: 41460

American (AMR) AF: 0.272 AC: 4164 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.419 AC: 1454 AN: 3470

East Asian (EAS) AF: 0.231 AC: 1194 AN: 5174

South Asian (SAS) AF: 0.394 AC: 1897 AN: 4820

European-Finnish (FIN) AF: 0.313 AC: 3307 AN: 10556

Middle Eastern (MID) AF: 0.364 AC: 107 AN: 294

European-Non Finnish (NFE) AF: 0.327 AC: 22254 AN: 67970

Other (OTH) AF: 0.328 AC: 694 AN: 2114

Alfa AF: 0.316 Hom.: 11503

Bravo AF: 0.317

Asia WGS AF: 0.337 AC: 1171 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	2.7
DANN	Benign	0.70
PhyloP100		-0.30
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs9746695; hg19: chr16-11207894;