rs67752076

chrX-38352697-A-GchrX-38352697-A-T

Variant summary

Our verdict is Pathogenic. Variant got 13 ACMG points: 13P and 0B. PVS1 PS1_Moderate PM2 PP5

The NM_000531.6(OTC):c.1A>G(p.Met1?) variant causes a start lost change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Pathogenic (no stars).

• Frequency: Genomes: not found (cov: 23)
• Consequence: OTC NM_000531.6 start_lost
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 4.73

Genes affected

OTC (HGNC:8512): (ornithine transcarbamylase) This nuclear gene encodes a mitochondrial matrix enzyme. The encoded protein is involved in the urea cycle which functions to detoxify ammonia into urea for excretion. Mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia. [provided by RefSeq, May 2022]

ACMG classification

Verdict is Pathogenic. Variant got 13 ACMG points.

• PVS1: Start lost variant, no new inframe start found.
• PS1: Another start lost variant in NM_000531.6 (OTC) was described as [Pathogenic] in ClinVar as 97131
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant X-38352697-A-G is Pathogenic according to our data. Variant chrX-38352697-A-G is described in ClinVar as [Pathogenic]. Clinvar id is 97130.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
OTC	NM_000531.6	c.1A>G	p.Met1?	start_lost	1/10	ENST00000039007.5
OTC	NM_001407092.1	c.1A>G	p.Met1?	start_lost	3/12
OTC	XM_017029556.2	c.1A>G	p.Met1?	start_lost	1/9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
OTC	ENST00000039007.5	c.1A>G	p.Met1?	start_lost	1/10	1	NM_000531.6	P1
OTC	ENST00000488812.1	n.93A>G		non_coding_transcript_exon_variant	1/6	5
OTC	ENST00000643344.1	c.1A>G	p.Met1?	start_lost, NMD_transcript_variant	1/11

Frequencies

GnomAD3 genomes Cov.: 23

GnomAD4 exome Cov.: 26

GnomAD4 genome Cov.: 23

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

not provided Pathogenic:1

Pathogenic, no assertion criteria provided

literature only

GenMed Metabolism Lab

-

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Pathogenic	0.64	D
BayesDel_noAF	Pathogenic	0.68
Cadd	Benign	19
Dann	Uncertain	0.98
DEOGEN2	Benign	0.37	T
FATHMM_MKL	Pathogenic	0.97	D
LIST_S2	Uncertain	0.90	D
M_CAP	Pathogenic	1.0	D
MetaRNN	Pathogenic	0.99	D
MetaSVM	Pathogenic	0.86	D
MutationTaster	Benign	1.0	D
PROVEAN	Benign	-0.58	N
REVEL	Uncertain	0.64
Sift	Benign	0.11	T
Sift4G	Benign	0.18	T
Polyphen		0.064	B
Vest4		0.96
MutPred		0.97		Loss of helix (P = 0.0626);
MVP		1.0
ClinPred		0.97	D
GERP RS		5.9
Varity_R		0.43
gMVP		0.88

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

Publications

LitVar

Other links and lift over

dbSNP: rs67752076; hg19: chrX-38211950;