7-151381734-C-G

Variant names:

• chr7-151381734-C-G
• rs1210963311
• NM_198285.3:c.979G>C

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_198285.3(WDR86):​c.979G>C​(p.Val327Leu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 12/19 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. V327M) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 34)
• Consequence: WDR86 NM_198285.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.430
• Publications: 0 publications found

Genes affected

WDR86 (HGNC:28020): (WD repeat domain 86)

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.16114214).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_198285.3. 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
	WDR86	NM_198285.3	MANE Select	c.979G>C	p.Val327Leu	missense	Exon 6 of 6	NP_938026.2	Q86TI4-3
	WDR86	NM_001284260.2		c.1043G>C	p.Gly348Ala	missense	Exon 6 of 6	NP_001271189.1	Q86TI4-4
	WDR86	NM_001284261.2		c.459G>C	p.Arg153Ser	missense	Exon 5 of 5	NP_001271190.1	Q86TI4-2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	WDR86	ENST00000334493.11	TSL:5 MANE Select	c.979G>C	p.Val327Leu	missense	Exon 6 of 6	ENSP00000335522.7	Q86TI4-3
	WDR86	ENST00000469830.2	TSL:2	c.1043G>C	p.Gly348Ala	missense	Exon 6 of 6	ENSP00000419162.2	Q86TI4-4
	WDR86	ENST00000477459.5	TSL:2	c.459G>C	p.Arg153Ser	missense	Exon 5 of 5	ENSP00000417512.1	Q86TI4-2

Frequencies

GnomAD3 genomes Cov.: 34

GnomAD4 exome Cov.: 54

GnomAD4 genome Cov.: 34

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.15
BayesDel_addAF	Uncertain	0.079	D
BayesDel_noAF	Benign	-0.28
CADD	Benign	18
DANN	Uncertain	0.99
Eigen	Benign	-0.63
Eigen_PC	Benign	-0.37
FATHMM_MKL	Benign	0.21	N
LIST_S2	Benign	0.41	T
M_CAP	Pathogenic	0.52	D
MetaRNN	Benign	0.16	T
MetaSVM	Benign	-1.0	T
PhyloP100		0.43
PROVEAN	Benign	-1.4	N
REVEL	Benign	0.10
Sift	Pathogenic	0.0	D
Sift4G	Benign	0.57	T
Vest4		0.20
MutPred		0.38		Gain of helix (P = 0.0425)
MVP		0.48
ClinPred		0.64	D
GERP RS		3.6
Varity_R		0.12
gMVP		0.37
Mutation Taster		=90/10	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

dbSNP: rs1210963311; hg19: chr7-151078820;