rs370545053

Variant names:

• chr16-23068519-C-A
• NM_020718.4:c.3586G>T

Your query was ambiguous. Multiple possible variants found:

• chr16-23068519-C-A
• chr16-23068519-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_020718.4(USP31):​c.3586G>T​(p.Val1196Leu) 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. 13/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: USP31 NM_020718.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 3.54

Genes affected

USP31 (HGNC:20060): (ubiquitin specific peptidase 31) Enables thiol-dependent deubiquitinase. Involved in protein deubiquitination. Located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.15275845).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
USP31	NM_020718.4	c.3586G>T	p.Val1196Leu	missense_variant	Exon 16 of 16	ENST00000219689.12	NP_065769.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
USP31	ENST00000219689.12	c.3586G>T	p.Val1196Leu	missense_variant	Exon 16 of 16	1	NM_020718.4	ENSP00000219689.7
USP31	ENST00000567975.1	c.1465G>T	p.Val489Leu	missense_variant	Exon 2 of 2	2		ENSP00000461621.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 40

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.15
BayesDel_addAF	Benign	-0.13	T
BayesDel_noAF	Benign	-0.42
CADD	Benign	11
DANN	Benign	0.97
DEOGEN2	Benign	0.014	T;.
Eigen	Benign	-0.10
Eigen_PC	Benign	-0.054
FATHMM_MKL	Uncertain	0.92	D
LIST_S2	Uncertain	0.88	D;D
M_CAP	Benign	0.0065	T
MetaRNN	Benign	0.15	T;T
MetaSVM	Benign	-0.98	T
MutationAssessor	Uncertain	2.4	M;.
PrimateAI	Uncertain	0.51	T
PROVEAN	Benign	-0.38	N;.
REVEL	Benign	0.081
Sift	Benign	0.067	T;.
Sift4G	Benign	0.32	T;T
Polyphen		0.13	B;.
Vest4		0.18
MutPred		0.26		Loss of sheet (P = 0.0315);.;
MVP		0.61
MPC		0.33
ClinPred		0.42	T
GERP RS		4.8
Varity_R		0.047
gMVP		0.22

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

No publications associated with this variant yet.

Other links and lift over

hg19: chr16-23079840;