6-158980866-C-T

Position:

chr6-158980866-C-T

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBS1BS2

The NM_031924.8(RSPH3):c.767G>A(p.Arg256Gln) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0213 in 1,614,062 control chromosomes in the GnomAD database, including 415 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.018 ( 34 hom., cov: 32)

Exomes 𝑓: 0.022 ( 381 hom. )

Consequence

RSPH3
NM_031924.8 missense

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:4

Conservation

PhyloP100: 0.792

Variant links:

Genes affected

RSPH3 (HGNC:21054): (radial spoke head 3) The protein encoded by this gene acts as a protein kinase A anchoring protein. Mutations in this gene cause primary ciliary dyskinesia; a disorder characterized by defects of the axoneme in motile cilia and sperm flagella. The homolog of this gene was first identified in the blue-green algae Chlamydomonas as encoding a radial spoke protein that formed a structural component of motile cilia and flagella. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016]

RSPH3 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -20 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.0036847591).

BP6

Variant 6-158980866-C-T is Benign according to our data. Variant chr6-158980866-C-T is described in ClinVar as [Likely_benign]. Clinvar id is 475820.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr6-158980866-C-T is described in Lovd as [Likely_benign]. Variant chr6-158980866-C-T is described in Lovd as [Benign].

BS1

Variant frequency is greater than expected in population nfe. gnomad4 allele frequency = 0.0178 (2709/152254) while in subpopulation NFE AF= 0.0237 (1612/68012). AF 95% confidence interval is 0.0227. There are 34 homozygotes in gnomad4. There are 1287 alleles in male gnomad4 subpopulation. Median coverage is 32. This position pass quality control queck.

BS2

High Homozygotes in GnomAd4 at 34 AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RSPH3	NM_031924.8 linkuse as main transcript	c.767G>A	p.Arg256Gln	missense_variant	6/8	ENST00000367069.7	NP_114130.4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RSPH3	ENST00000367069.7 linkuse as main transcript	c.767G>A	p.Arg256Gln	missense_variant	6/8	1	NM_031924.8	ENSP00000356036	P1
RSPH3	ENST00000449822.5 linkuse as main transcript	c.479G>A	p.Arg160Gln	missense_variant	4/6	2		ENSP00000393195

Frequencies

GnomAD3 genomes

AF:

0.0178

AC:

2707

AN:

152136

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00929

Gnomad AMI

AF:

0.0934

Gnomad AMR

AF:

0.0234

Gnomad ASJ

AF:

0.00662

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00850

Gnomad FIN

AF:

0.0155

Gnomad MID

AF:

0.0253

Gnomad NFE

AF:

0.0237

Gnomad OTH

AF:

0.0158

GnomAD3 exomes

AF:

0.0167

AC:

4211

AN:

251470

Hom.:

AF XY:

0.0171

AC XY:

2320

AN XY:

135904

show subpopulations

Gnomad AFR exome

AF:

0.00886

Gnomad AMR exome

AF:

0.0145

Gnomad ASJ exome

AF:

0.00695

Gnomad EAS exome

AF:

0.000326

Gnomad SAS exome

AF:

0.0137

Gnomad FIN exome

AF:

0.0164

Gnomad NFE exome

AF:

0.0229

Gnomad OTH exome

AF:

0.0171

GnomAD4 exome

AF:

0.0216

AC:

31621

AN:

1461808

Hom.:

381

Cov.:

AF XY:

0.0213

AC XY:

15456

AN XY:

727206

show subpopulations

Gnomad4 AFR exome

AF:

0.0101

Gnomad4 AMR exome

AF:

0.0152

Gnomad4 ASJ exome

AF:

0.00746

Gnomad4 EAS exome

AF:

0.000227

Gnomad4 SAS exome

AF:

0.0127

Gnomad4 FIN exome

AF:

0.0155

Gnomad4 NFE exome

AF:

0.0245

Gnomad4 OTH exome

AF:

0.0187

GnomAD4 genome

AF:

0.0178

AC:

2709

AN:

152254

Hom.:

Cov.:

AF XY:

0.0173

AC XY:

1287

AN XY:

74452

show subpopulations

Gnomad4 AFR

AF:

0.00931

Gnomad4 AMR

AF:

0.0233

Gnomad4 ASJ

AF:

0.00662

Gnomad4 EAS

AF:

0.00

Gnomad4 SAS

AF:

0.00851

Gnomad4 FIN

AF:

0.0155

Gnomad4 NFE

AF:

0.0237

Gnomad4 OTH

AF:

0.0156

Alfa

AF:

0.0220

Hom.:

Bravo

AF:

0.0179

TwinsUK

AF:

0.0213

AC:

ALSPAC

AF:

0.0236

AC:

ESP6500AA

AF:

0.0113

AC:

ESP6500EA

AF:

0.0245

AC:

211

ExAC

AF:

0.0167

AC:

2026

Asia WGS

AF:

0.00491

AC:

AN:

3478

EpiCase

AF:

0.0250

EpiControl

AF:

0.0240

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:4

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

Primary ciliary dyskinesia 32

Benign:2

Benign, criteria provided, single submitter	clinical testing	ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	Nov 09, 2023	- -
Benign, criteria provided, single submitter	clinical testing	Labcorp Genetics (formerly Invitae), Labcorp	Jan 31, 2024	- -

not provided

Benign:2

Likely benign, criteria provided, single submitter	not provided	Breakthrough Genomics, Breakthrough Genomics	-	- -
Likely benign, criteria provided, single submitter	clinical testing	GeneDx	Oct 13, 2020	- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.085

BayesDel_addAF

Benign

-0.59

BayesDel_noAF

Benign

-0.60

CADD

Benign

DANN

Uncertain

0.99

DEOGEN2

Benign

0.056

T;.;T

Eigen

Benign

-0.85

Eigen_PC

Benign

-0.96

FATHMM_MKL

Benign

0.12

LIST_S2

Uncertain

0.86

D;D;D

MetaRNN

Benign

0.0037

T;T;T

MetaSVM

Benign

-0.97

MutationAssessor

Uncertain

2.1

.;.;M

MutationTaster

Benign

1.0

N;N;N;N

PrimateAI

Benign

0.21

PROVEAN

Uncertain

-2.6

D;D;D

REVEL

Benign

0.037

Sift

Benign

0.22

T;T;T

Sift4G

Benign

0.15

T;T;T

Polyphen

0.10

.;.;B

Vest4

0.12

MPC

0.39

ClinPred

0.025

GERP RS

-0.62

Varity_R

0.053

gMVP

0.57

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