chr12-14789076-C-T

Variant names:

• chr12-14789076-C-T
• NM_016312.3:c.1367G>A

Variant summary

Our verdict is Uncertain significance. The variant received 1 ACMG points: 2P and 1B. PM2 BP4

The NM_016312.3(WBP11):​c.1367G>A​(p.Arg456Gln) variant causes a missense change. The variant allele was found at a frequency of 0.00000146 in 1,365,298 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency:
  • Genomes: not found (cov: 32)
  • Exomes 𝑓: 0.0000015 (0 hom.)
• Consequence: WBP11 NM_016312.3 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 6.95
• Publications: 0 publications found

Genes affected

WBP11 (HGNC:16461): (WW domain binding protein 11) This gene encodes a nuclear protein, which colocalizes with mRNA splicing factors and intermediate filament-containing perinuclear networks. This protein has 95% amino acid sequence identity to the mouse Wbp11 protein. It contains two proline-rich regions that bind to the WW domain of Npw38, a nuclear protein, and thus this protein is also called Npw38-binding protein NpwBP. The Npw38-NpwBP complex may function as a component of an mRNA factory in the nucleus. [provided by RefSeq, Jul 2008]

GUCY2C-AS1 (HGNC:56054): (GUCY2C antisense RNA 1)

ACMG classification

Our verdict: Uncertain_significance. The variant received 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.41406333).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_016312.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	WBP11	NM_016312.3	MANE Select	c.1367G>A	p.Arg456Gln	missense	Exon 11 of 12	NP_057396.1	Q9Y2W2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	WBP11	ENST00000261167.7	TSL:1 MANE Select	c.1367G>A	p.Arg456Gln	missense	Exon 11 of 12	ENSP00000261167.2	Q9Y2W2
	WBP11	ENST00000858075.1		c.1367G>A	p.Arg456Gln	missense	Exon 12 of 13	ENSP00000528134.1
	WBP11	ENST00000918140.1		c.1367G>A	p.Arg456Gln	missense	Exon 11 of 12	ENSP00000588199.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome AF: 0.00000146 AC: 2 AN: 1365298 Hom.: 0 Cov.: 31 AF XY: 0.00000296 AC XY: 2 AN XY: 676532

African (AFR) AF: 0.00 AC: 0 AN: 26742

American (AMR) AF: 0.00 AC: 0 AN: 22214

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 22760

East Asian (EAS) AF: 0.00 AC: 0 AN: 32250

South Asian (SAS) AF: 0.00 AC: 0 AN: 68416

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 52710

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 5478

European-Non Finnish (NFE) AF: 9.27e-7 AC: 1 AN: 1078374

Other (OTH) AF: 0.0000177 AC: 1 AN: 56354

GnomAD4 genome Cov.: 32

ClinVar

ClinVar submissions

Significance: Uncertain significance

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	1	-	Inborn genetic diseases (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.84
BayesDel_addAF	Uncertain	0.054	T
BayesDel_noAF	Benign	-0.16
CADD	Uncertain	25
DANN	Uncertain	0.99
DEOGEN2	Benign	0.041	T
Eigen	Uncertain	0.44
Eigen_PC	Uncertain	0.49
FATHMM_MKL	Pathogenic	0.97	D
LIST_S2	Benign	0.85	T
M_CAP	Benign	0.021	T
MetaRNN	Benign	0.41	T
MetaSVM	Uncertain	0.057	D
MutationAssessor	Benign	1.9	L
PhyloP100		7.0
PrimateAI	Pathogenic	0.81	D
PROVEAN	Benign	-1.1	N
REVEL	Uncertain	0.35
Sift	Benign	0.36	T
Sift4G	Benign	0.34	T
Polyphen		0.99	D
Vest4		0.59
MutPred		0.21		Loss of methylation at R456 (P = 0.0817)
MVP		0.29
MPC		0.67
ClinPred		0.90	D
GERP RS		4.7
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.091
gMVP		0.31
Mutation Taster		=83/17	polymorphism

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

hg19: chr12-14942010;