chr16-56351496-T-A

Variant names:

• chr16-56351496-T-A
• rs587777054
• NM_020988.3:c.836T>A

Variant summary

Our verdict is Likely pathogenic. The variant received 9 ACMG points: 9P and 0B. PM1 PM2 PP3_Strong PP5

The NM_020988.3(GNAO1):​c.836T>A​(p.Ile279Asn) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. 12/20 in silico tools predict a damaging outcome for this variant. Variant has been reported in ClinVar as Pathogenic (no stars).

• Frequency: Genomes: not found (cov: 33)
• Consequence: GNAO1 NM_020988.3 missense
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 8.02
• Publications: 12 publications found

Genes affected

GNAO1 (HGNC:4389): (G protein subunit alpha o1) The protein encoded by this gene represents the alpha subunit of the Go heterotrimeric G-protein signal-transducing complex. Defects in this gene are a cause of early-onset epileptic encephalopathy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]

GNAO1 Gene-Disease associations (from GenCC):

• developmental and epileptic encephalopathy, 17

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics
• genetic developmental and epileptic encephalopathy

  Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: Orphanet, ClinGen
• movement disorder

  Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen, Illumina
• neurodevelopmental disorder with involuntary movements

  Inheritance: AD Classification: STRONG Submitted by: Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Likely_pathogenic. The variant received 9 ACMG points.

• PM1: In a hotspot region, there are 7 aminoacids with missense pathogenic changes in the window of +-8 aminoacids around while only 1 benign, 7 uncertain in NM_020988.3
• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.982
• PP5: Variant 16-56351496-T-A is Pathogenic according to our data. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr16-56351496-T-A is described in CliVar as Pathogenic. Clinvar id is 66112.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GNAO1	NM_020988.3	c.836T>A	p.Ile279Asn	missense_variant	Exon 7 of 9	ENST00000262493.12	NP_066268.1
GNAO1	XM_011523003.4	c.710T>A	p.Ile237Asn	missense_variant	Exon 7 of 9		XP_011521305.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GNAO1	ENST00000262493.12	c.836T>A	p.Ile279Asn	missense_variant	Exon 7 of 9	1	NM_020988.3	ENSP00000262493.6

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 33

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Developmental and epileptic encephalopathy, 17 Pathogenic:1

Sep 05, 2013

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.98
BayesDel_addAF	Pathogenic	0.34	D
BayesDel_noAF	Pathogenic	0.25
CADD	Pathogenic	29
DANN	Uncertain	0.99
DEOGEN2	Pathogenic	0.94	D;D;.;.;.
Eigen	Pathogenic	1.0
Eigen_PC	Pathogenic	0.95
FATHMM_MKL	Pathogenic	0.98	D
LIST_S2	Uncertain	0.97	.;D;D;D;D
M_CAP	Pathogenic	0.83	D
MetaRNN	Pathogenic	0.98	D;D;D;D;D
MetaSVM	Pathogenic	1.1	D
MutationAssessor	Pathogenic	4.1	H;H;.;.;.
PhyloP100		8.0
PROVEAN	Pathogenic	-6.6	D;.;.;.;.
REVEL	Pathogenic	0.93
Sift	Pathogenic	0.0	D;.;.;.;.
Sift4G	Pathogenic	0.0	D;.;.;.;.
Polyphen		1.0	D;D;.;.;.
Vest4		0.95
MutPred		0.85		Gain of disorder (P = 0.0152);Gain of disorder (P = 0.0152);.;.;.;
MVP		0.91
ClinPred		1.0	D
GERP RS		5.9
Varity_R		0.92
Mutation Taster		=3/97	disease causing (ClinVar)

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

Other links and lift over

dbSNP: rs587777054; hg19: chr16-56385408;