dbSNP rs140532446: MOV10L1:p.Ala131Thr (chr22-50099551-G-A) – ACMG Classification: Benign (-10 pts)

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_StrongBP6_ModerateBS2

The NM_018995.3(MOV10L1):c.391G>A(p.Ala131Thr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00615 in 1,614,188 control chromosomes in the GnomAD database, including 56 homozygotes. In-silico tool predicts a benign outcome for this variant. 13/20 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

Frequency

Genomes: 𝑓 0.0051 ( 9 hom., cov: 32)

Exomes 𝑓: 0.0063 ( 47 hom. )

Consequence

MOV10L1
NM_018995.3 missense

Scores

Clinical Significance

Benign criteria provided, single submitter B:1

Conservation

PhyloP100: 2.11

Variant links:

Genes affected

MOV10L1 (HGNC:7201): (Mov10 like RNA helicase 1) This gene is similar to a mouse gene that encodes a putative RNA helicase and shows testis-specific expression. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]

MOV10L1 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -10 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.009549081).

BP6

Variant 22-50099551-G-A is Benign according to our data. Variant chr22-50099551-G-A is described in ClinVar as [Benign]. Clinvar id is 2653363.Status of the report is criteria_provided_single_submitter, 1 stars.

BS2

High Homozygotes in GnomAd4 at 9 AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MOV10L1	NM_018995.3 link	c.391G>A	p.Ala131Thr	missense_variant	Exon 3 of 27	ENST00000262794.10	NP_061868.1	Q9BXT6-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MOV10L1	ENST00000262794.10 link	c.391G>A	p.Ala131Thr	missense_variant	Exon 3 of 27	1	NM_018995.3	ENSP00000262794.5		Q9BXT6-1

Frequencies

GnomAD3 genomes

AF:

0.00510

AC:

777

AN:

152222

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.000820

Gnomad AMI

AF:

0.0175

Gnomad AMR

AF:

0.00399

Gnomad ASJ

AF:

0.00518

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.0106

Gnomad FIN

AF:

0.00471

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.00789

Gnomad OTH

AF:

0.00478

GnomAD3 exomes

AF:

0.00596

AC:

1499

AN:

251412

Hom.:

AF XY:

0.00657

AC XY:

893

AN XY:

135868

show subpopulations

Gnomad AFR exome

AF:

0.000923

Gnomad AMR exome

AF:

0.00124

Gnomad ASJ exome

AF:

0.00377

Gnomad EAS exome

AF:

0.00

Gnomad SAS exome

AF:

0.0124

Gnomad FIN exome

AF:

0.00522

Gnomad NFE exome

AF:

0.00769

Gnomad OTH exome

AF:

0.00587

GnomAD4 exome

AF:

0.00626

AC:

9145

AN:

1461848

Hom.:

Cov.:

AF XY:

0.00661

AC XY:

4806

AN XY:

727220

show subpopulations

Gnomad4 AFR exome

AF:

0.00108

Gnomad4 AMR exome

AF:

0.00136

Gnomad4 ASJ exome

AF:

0.00444

Gnomad4 EAS exome

AF:

0.0000252

Gnomad4 SAS exome

AF:

0.0119

Gnomad4 FIN exome

AF:

0.00507

Gnomad4 NFE exome

AF:

0.00655

Gnomad4 OTH exome

AF:

0.00538

GnomAD4 genome

AF:

0.00511

AC:

779

AN:

152340

Hom.:

Cov.:

AF XY:

0.00498

AC XY:

371

AN XY:

74496

show subpopulations

Gnomad4 AFR

AF:

0.000818

Gnomad4 AMR

AF:

0.00399

Gnomad4 ASJ

AF:

0.00518

Gnomad4 EAS

AF:

0.00

Gnomad4 SAS

AF:

0.0110

Gnomad4 FIN

AF:

0.00471

Gnomad4 NFE

AF:

0.00789

Gnomad4 OTH

AF:

0.00473

Alfa

AF:

0.00684

Hom.:

Bravo

AF:

0.00414

TwinsUK

AF:

0.00512

AC:

ALSPAC

AF:

0.00545

AC:

ESP6500AA

AF:

0.000908

AC:

ESP6500EA

AF:

0.00674

AC:

ExAC

AF:

0.00630

AC:

765

Asia WGS

AF:

0.00520

AC:

AN:

3478

EpiCase

AF:

0.00665

EpiControl

AF:

0.00658

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

not provided

Benign:1

Dec 01, 2022

CeGaT Center for Human Genetics Tuebingen

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

MOV10L1: BP4, BS1, BS2 -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.080

BayesDel_addAF

Benign

-0.58

BayesDel_noAF

Benign

-0.60

CADD

Benign

DANN

Uncertain

0.98

DEOGEN2

Benign

0.068

T;T;.;.

Eigen

Benign

-0.44

Eigen_PC

Benign

-0.42

FATHMM_MKL

Benign

0.65

LIST_S2

Benign

0.61

T;.;T;T

MetaRNN

Benign

0.0095

T;T;T;T

MetaSVM

Benign

-1.0

MutationAssessor

Benign

0.99

L;L;L;.

PrimateAI

Benign

0.32

PROVEAN

Benign

-1.6

N;N;N;N

REVEL

Benign

0.035

Sift

Benign

0.13

T;T;T;T

Sift4G

Benign

0.28

T;T;T;T

Polyphen

0.060

B;B;.;.

Vest4

0.13

MVP

0.39

MPC

0.089

ClinPred

0.0055

GERP RS

3.6

Varity_R

0.062

gMVP

0.23

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over