rs2282542

Variant names:

• chr18-13056683-G-A
• rs2282542
• NM_032142.4:c.4093G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_032142.4(CEP192):​c.4093G>A​(p.Val1365Met) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.136 in 1,601,634 control chromosomes in the GnomAD database, including 16,645 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/20 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: 𝑓 0.14 (1589 hom., cov: 33)
  • Exomes 𝑓: 0.14 (15056 hom.)
• Consequence: CEP192 NM_032142.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.561
• Publications: 27 publications found

Genes affected

CEP192 (HGNC:25515): (centrosomal protein 192) Enables phosphatase binding activity. Involved in centrosome-templated microtubule nucleation; mitotic spindle assembly; and protein localization to centrosome. Located in centriole; centrosome; and cytosol. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (MetaRNN=0.0037734509).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.301 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_032142.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CEP192	NM_032142.4	MANE Select	c.4093G>A	p.Val1365Met	missense	Exon 19 of 45	NP_115518.3

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CEP192	ENST00000506447.5	TSL:5 MANE Select	c.4093G>A	p.Val1365Met	missense	Exon 19 of 45	ENSP00000427550.1
	CEP192	ENST00000511820.6	TSL:1	c.2707G>A	p.Val903Met	missense	Exon 9 of 35	ENSP00000467038.1
	CEP192	ENST00000510237.5	TSL:1	n.2893G>A		non_coding_transcript_exon	Exon 10 of 35	ENSP00000423147.1

Frequencies

GnomAD3 genomes AF: 0.137 AC: 20878 AN: 152120 Hom.: 1587 Cov.: 33

Gnomad AFR AF: 0.121

Gnomad AMI AF: 0.0866

Gnomad AMR AF: 0.126

Gnomad ASJ AF: 0.192

Gnomad EAS AF: 0.313

Gnomad SAS AF: 0.248

Gnomad FIN AF: 0.119

Gnomad MID AF: 0.149

Gnomad NFE AF: 0.129

Gnomad OTH AF: 0.151

GnomAD2 exomes AF: 0.153 AC: 36168 AN: 236220 AF XY: 0.156

Gnomad AFR exome AF: 0.123

Gnomad AMR exome AF: 0.105

Gnomad ASJ exome AF: 0.196

Gnomad EAS exome AF: 0.316

Gnomad FIN exome AF: 0.122

Gnomad NFE exome AF: 0.127

Gnomad OTH exome AF: 0.150

GnomAD4 exome AF: 0.136 AC: 197403 AN: 1449396 Hom.: 15056 Cov.: 33 AF XY: 0.139 AC XY: 100165 AN XY: 720618

African (AFR) AF: 0.124 AC: 4089 AN: 32926

American (AMR) AF: 0.104 AC: 4398 AN: 42332

Ashkenazi Jewish (ASJ) AF: 0.190 AC: 4766 AN: 25122

East Asian (EAS) AF: 0.284 AC: 11273 AN: 39624

South Asian (SAS) AF: 0.227 AC: 19068 AN: 84064

European-Finnish (FIN) AF: 0.124 AC: 6575 AN: 53060

Middle Eastern (MID) AF: 0.178 AC: 1013 AN: 5678

European-Non Finnish (NFE) AF: 0.124 AC: 136930 AN: 1106744

Other (OTH) AF: 0.155 AC: 9291 AN: 59846

GnomAD4 genome AF: 0.137 AC: 20892 AN: 152238 Hom.: 1589 Cov.: 33 AF XY: 0.140 AC XY: 10401 AN XY: 74452

African (AFR) AF: 0.121 AC: 5030 AN: 41532

American (AMR) AF: 0.126 AC: 1924 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.192 AC: 667 AN: 3472

East Asian (EAS) AF: 0.313 AC: 1620 AN: 5170

South Asian (SAS) AF: 0.248 AC: 1199 AN: 4832

European-Finnish (FIN) AF: 0.119 AC: 1266 AN: 10598

Middle Eastern (MID) AF: 0.139 AC: 41 AN: 294

European-Non Finnish (NFE) AF: 0.129 AC: 8741 AN: 68016

Other (OTH) AF: 0.154 AC: 325 AN: 2114

Alfa AF: 0.135 Hom.: 7097

Bravo AF: 0.135

TwinsUK AF: 0.120 AC: 444

ALSPAC AF: 0.119 AC: 459

ESP6500AA AF: 0.119 AC: 524

ESP6500EA AF: 0.127 AC: 1096

ExAC AF: 0.151 AC: 18303

Asia WGS AF: 0.265 AC: 921 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.068
BayesDel_addAF	Benign	-0.83	T
BayesDel_noAF	Benign	-0.82
CADD	Benign	0.25
DANN	Benign	0.073
DEOGEN2	Benign	0.0028	T
Eigen	Benign	-1.8
Eigen_PC	Benign	-1.8
FATHMM_MKL	Benign	0.0066	N
LIST_S2	Benign	0.073	T
MetaRNN	Benign	0.0038	T
MetaSVM	Benign	-0.97	T
PhyloP100		-0.56
PrimateAI	Benign	0.25	T
PROVEAN	Benign	0.49	N
REVEL	Benign	0.0080
Sift	Benign	1.0	T
Sift4G	Benign	0.59	T
Vest4		0.031
MPC		0.097
ClinPred		0.00026	T
GERP RS		-2.5
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Varity_R		0.017
gMVP		0.16
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs2282542; hg19: chr18-13056682; COSMIC: COSV58059891; COSMIC: COSV58059891;