rs2028574

chr3-191375386-T-Achr3-191375386-T-G

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_178335.3(CCDC50):c.773T>A(p.Ile258Asn) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.408 in 1,613,192 control chromosomes in the GnomAD database, including 138,251 homozygotes. In-silico tool predicts a benign outcome for this variant. 10/14 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.48 (18937 hom., cov: 31)
  • Exomes 𝑓: 0.40 (119314 hom.)
• Consequence: CCDC50 NM_178335.3 missense
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:5
• Conservation: PhyloP100: -0.428

Genes affected

CCDC50 (HGNC:18111): (coiled-coil domain containing 50) This gene encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule-based structures. This protein may also function as a negative regulator of NF-kB signaling and as an effector of epidermal growth factor (EGF)-mediated cell signaling. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (MetaRNN=2.1176315E-6).
• BP6: Variant 3-191375386-T-A is Benign according to our data. Variant chr3-191375386-T-A is described in ClinVar as [Benign]. Clinvar id is 48158.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr3-191375386-T-A is described in Lovd as [Benign].
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.676 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CCDC50	NM_178335.3	c.773T>A	p.Ile258Asn	missense_variant	6/12	ENST00000392455.9
CCDC50	XM_011512460.2	c.773T>A	p.Ile258Asn	missense_variant	6/8
CCDC50	NM_174908.4	c.449-4773T>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CCDC50	ENST00000392455.9	c.773T>A	p.Ile258Asn	missense_variant	6/12	1	NM_178335.3	P3
CCDC50	ENST00000392456.4	c.449-4773T>A		intron_variant		1		A1

Frequencies

GnomAD3 genomes AF: 0.483 AC: 73376 AN: 151854 Hom.: 18910 Cov.: 31

Gnomad AFR AF: 0.683

Gnomad AMI AF: 0.258

Gnomad AMR AF: 0.473

Gnomad ASJ AF: 0.461

Gnomad EAS AF: 0.456

Gnomad SAS AF: 0.352

Gnomad FIN AF: 0.374

Gnomad MID AF: 0.456

Gnomad NFE AF: 0.397

Gnomad OTH AF: 0.459

GnomAD3 exomes AF: 0.428 AC: 106843 AN: 249772 Hom.: 23583 AF XY: 0.416 AC XY: 56108 AN XY: 134982

Gnomad AFR exome AF: 0.683

Gnomad AMR exome AF: 0.497

Gnomad ASJ exome AF: 0.461

Gnomad EAS exome AF: 0.454

Gnomad SAS exome AF: 0.353

Gnomad FIN exome AF: 0.371

Gnomad NFE exome AF: 0.395

Gnomad OTH exome AF: 0.416

GnomAD4 exome AF: 0.401 AC: 585516 AN: 1461218 Hom.: 119314 Cov.: 58 AF XY: 0.398 AC XY: 289076 AN XY: 726876

Gnomad4 AFR exome AF: 0.684

Gnomad4 AMR exome AF: 0.496

Gnomad4 ASJ exome AF: 0.459

Gnomad4 EAS exome AF: 0.410

Gnomad4 SAS exome AF: 0.360

Gnomad4 FIN exome AF: 0.368

Gnomad4 NFE exome AF: 0.391

Gnomad4 OTH exome AF: 0.414

GnomAD4 genome AF: 0.483 AC: 73464 AN: 151974 Hom.: 18937 Cov.: 31 AF XY: 0.482 AC XY: 35785 AN XY: 74270

Gnomad4 AFR AF: 0.683

Gnomad4 AMR AF: 0.473

Gnomad4 ASJ AF: 0.461

Gnomad4 EAS AF: 0.455

Gnomad4 SAS AF: 0.352

Gnomad4 FIN AF: 0.374

Gnomad4 NFE AF: 0.397

Gnomad4 OTH AF: 0.458

Alfa AF: 0.416 Hom.: 10216

Bravo AF: 0.503

TwinsUK AF: 0.385 AC: 1426

ALSPAC AF: 0.398 AC: 1532

ESP6500AA AF: 0.671 AC: 2955

ESP6500EA AF: 0.396 AC: 3404

ExAC AF: 0.427 AC: 51829

Asia WGS AF: 0.440 AC: 1530 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:5

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not specified Benign:3

Benign, criteria provided, single submitter	clinical testing	PreventionGenetics, part of Exact Sciences	-	- -
Benign, criteria provided, single submitter	clinical testing	Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	May 07, 2012	Ile258Asn in Exon 06 of CCDC50: This variant is not expected to have clinical si gnificance because it has been identified in 39.5% (2775/7020) of European Ameri can chromosomes from a broad population by the NHLBI Exome Sequencing Project (h ttp://evs.gs.washington.edu/EVS; dbSNP rs2028574). -
Benign, criteria provided, single submitter	clinical testing	GeneDx	May 09, 2017	This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

Invitae

Jan 31, 2024

- -

Autosomal dominant nonsyndromic hearing loss 44 Benign:1

Benign, criteria provided, single submitter

clinical testing

Genome-Nilou Lab

Jul 14, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Benign	-0.83	T
BayesDel_noAF	Benign	-0.83
Cadd	Benign	0.85
Dann	Benign	0.24
Eigen	Benign	-1.4
Eigen_PC	Benign	-1.5
FATHMM_MKL	Benign	0.010	N
LIST_S2	Benign	0.21	T
MetaRNN	Benign	0.0000021	T
MetaSVM	Benign	-0.95	T
MutationTaster	Benign	1.0	P;P
PrimateAI	Benign	0.22	T
Polyphen		0.0	B
ClinPred		0.0011	T
GERP RS		-3.5
gMVP		0.045

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

Other links and lift over

dbSNP: rs2028574; hg19: chr3-191093175; COSMIC: COSV66668257;