rs11071033

Positions:

• chr15-54088003-T-C

Variant summary

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

The NM_001080534.3(UNC13C):​c.2984-55015T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.476 in 151,766 control chromosomes in the GnomAD database, including 18,706 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 0.48 (18706 hom., cov: 30)
• Consequence: UNC13C NM_001080534.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.657

Genes affected

UNC13C (HGNC:23149): (unc-13 homolog C) Predicted to enable calmodulin binding activity and syntaxin-1 binding activity. Predicted to be involved in several processes, including glutamatergic synaptic transmission; regulated exocytosis; and synaptic vesicle maturation. Predicted to be located in presynaptic active zone. Predicted to be active in several cellular components, including axon terminus; parallel fiber to Purkinje cell synapse; and presynaptic active zone cytoplasmic component. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.583 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
UNC13C	NM_001080534.3	c.2984-55015T>C		intron_variant		ENST00000260323.16	NP_001074003.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
UNC13C	ENST00000260323.16	c.2984-55015T>C		intron_variant		5	NM_001080534.3	ENSP00000260323	A1
UNC13C	ENST00000647821.1	c.2984-55015T>C		intron_variant				ENSP00000497525	P4

Frequencies

GnomAD3 genomes AF: 0.477 AC: 72291 AN: 151648 Hom.: 18713 Cov.: 30

Gnomad AFR AF: 0.285

Gnomad AMI AF: 0.671

Gnomad AMR AF: 0.460

Gnomad ASJ AF: 0.587

Gnomad EAS AF: 0.368

Gnomad SAS AF: 0.347

Gnomad FIN AF: 0.591

Gnomad MID AF: 0.430

Gnomad NFE AF: 0.588

Gnomad OTH AF: 0.502

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

GnomAD4 genome AF: 0.476 AC: 72282 AN: 151766 Hom.: 18706 Cov.: 30 AF XY: 0.473 AC XY: 35065 AN XY: 74178

Gnomad4 AFR AF: 0.285

Gnomad4 AMR AF: 0.460

Gnomad4 ASJ AF: 0.587

Gnomad4 EAS AF: 0.368

Gnomad4 SAS AF: 0.346

Gnomad4 FIN AF: 0.591

Gnomad4 NFE AF: 0.588

Gnomad4 OTH AF: 0.499

Alfa AF: 0.545 Hom.: 13503

Bravo AF: 0.459

Asia WGS AF: 0.355 AC: 1234 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	5.0
DANN	Benign	0.54

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: rs11071033; hg19: chr15-54380200;