chr2-210592937-C-T

Variant names:

Variant summary

Our verdict is Pathogenic. The variant received 10 ACMG points: 10P and 0B. PM2PP5_Very_Strong

The NM_001875.5(CPS1):c.1145C>T(p.Pro382Leu) variant causes a missense change. The variant allele was found at a frequency of 0.0000267 in 1,460,358 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Likely pathogenic (★★). Synonymous variant affecting the same amino acid position (i.e. P382P) has been classified as Likely benign.

Frequency

Genomes: not found (cov: 32)

Exomes 𝑓: 0.000027 ( 0 hom. )

Consequence

CPS1
NM_001875.5 missense

Scores

Clinical Significance

Likely pathogenic criteria provided, multiple submitters, no conflicts P:4U:1

Conservation

PhyloP100: 5.92

Publications

7 publications found

Variant links:

Genes affected

CPS1 (HGNC:2323): (carbamoyl-phosphate synthase 1) The mitochondrial enzyme encoded by this gene catalyzes synthesis of carbamoyl phosphate from ammonia and bicarbonate. This reaction is the first committed step of the urea cycle, which is important in the removal of excess urea from cells. The encoded protein may also represent a core mitochondrial nucleoid protein. Three transcript variants encoding different isoforms have been found for this gene. The shortest isoform may not be localized to the mitochondrion. Mutations in this gene have been associated with carbamoyl phosphate synthetase deficiency, susceptibility to persistent pulmonary hypertension, and susceptibility to venoocclusive disease after bone marrow transplantation.[provided by RefSeq, May 2010]

CPS1 Gene-Disease associations (from GenCC):

carbamoyl phosphate synthetase I deficiency disease
Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, G2P, Labcorp Genetics (formerly Invitae), ClinGen, Myriad Women’s Health

CPS1 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Pathogenic. The variant received 10 ACMG points.

PM2

Very rare variant in population databases, with high coverage;

PP5

Variant 2-210592937-C-T is Pathogenic according to our data. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-210592937-C-T is described in CliVar as Likely_pathogenic. Clinvar id is 550641.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CPS1	NM_001875.5 link	c.1145C>T	p.Pro382Leu	missense_variant	Exon 11 of 38	ENST00000233072.10	NP_001866.2	P31327-1A0A024R454Q6PEK7

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CPS1	ENST00000233072.10 link	c.1145C>T	p.Pro382Leu	missense_variant	Exon 11 of 38	1	NM_001875.5	ENSP00000233072.5		P31327-1

Frequencies

GnomAD3 genomes

Cov.:

GnomAD2 exomes

AF:

0.0000359

AC:

AN:

250886

AF XY:

0.0000516

show subpopulations

Gnomad AFR exome

AF:

0.00

Gnomad AMR exome

AF:

0.00

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.0000544

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.0000706

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.0000267

AC:

AN:

1460358

Hom.:

Cov.:

AF XY:

0.0000220

AC XY:

AN XY:

726514

show subpopulations

African (AFR)

AF:

0.0000300

AC:

AN:

33380

American (AMR)

AF:

0.00

AC:

AN:

44636

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26054

East Asian (EAS)

AF:

0.00

AC:

AN:

39672

South Asian (SAS)

AF:

0.0000116

AC:

AN:

86226

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53408

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5758

European-Non Finnish (NFE)

AF:

0.0000306

AC:

AN:

1110954

Other (OTH)

AF:

0.0000498

AC:

AN:

60270

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.457

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

Cov.:

Alfa

AF:

0.0000578

Hom.:

ExAC

AF:

0.0000247

AC:

EpiCase

AF:

0.0000546

EpiControl

AF:

0.000178

ClinVar

Significance: Likely pathogenic

Submissions summary: Pathogenic:4Uncertain:1

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

Congenital hyperammonemia, type I

Pathogenic:2Uncertain:1

Mar 06, 2021

The Laboratory of Genetics and Metabolism, Hunan Children’s Hospital

Significance:Likely pathogenic

Review Status:criteria provided, single submitter

Collection Method:research

- -

Feb 14, 2017

Counsyl

Significance:Uncertain significance

Review Status:no assertion criteria provided

Collection Method:clinical testing

This submission and the accompanying classification are no longer maintained by the submitter. For more information on current observations and classification, please contact variantquestions@myriad.com. -

Feb 26, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Likely pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

This sequence change replaces proline, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 382 of the CPS1 protein (p.Pro382Leu). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This missense change has been observed in individual(s) with clinical features of carbamoyl phosphate synthetase I deficiency (PMID: 21120950, 22173106, 31749211, 34298581). In at least one individual the data is consistent with being in trans (on the opposite chromosome) from a pathogenic variant. ClinVar contains an entry for this variant (Variation ID: 550641). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt CPS1 protein function with a negative predictive value of 95%. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. -

Pulmonary hypertension, neonatal, susceptibility to;C4082171:Congenital hyperammonemia, type I

Pathogenic:1

Apr 30, 2024

Fulgent Genetics, Fulgent Genetics

Significance:Likely pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Pulmonary hypertension, neonatal, susceptibility to

Pathogenic:1

Feb 20, 2024

Baylor Genetics

Significance:Likely pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.28

BayesDel_addAF

Pathogenic

0.28

BayesDel_noAF

Pathogenic

0.34

CADD

Pathogenic

(source)

DANN

Uncertain

1.0

DEOGEN2

Pathogenic

0.87

.;D;D

Eigen

Uncertain

0.68

Eigen_PC

Pathogenic

0.72

FATHMM_MKL

Uncertain

0.92

LIST_S2

Pathogenic

0.98

D;D;D

M_CAP

Benign

0.083

MetaRNN

Uncertain

0.66

D;D;D

MetaSVM

Uncertain

0.60

MutationAssessor

Pathogenic

3.2

.;M;.

PhyloP100

5.9

PrimateAI

Uncertain

0.60

PROVEAN

Pathogenic

-5.9

D;D;.

REVEL

Pathogenic

0.69

Sift

Uncertain

0.015

D;D;.

Sift4G

Uncertain

0.017

D;D;D

Polyphen

0.86

.;P;.

Vest4

0.65

MutPred

0.49

.;Loss of disorder (P = 0.0377);Loss of disorder (P = 0.0377);

MVP

0.95

MPC

0.34

ClinPred

0.86

GERP RS

6.0

PromoterAI

-0.024

Neutral

(source)

Varity_R

0.65

gMVP

0.89

Mutation Taster

=20/80

disease causing

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

Splicevardb

1.0

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over