20-58909186-C-G

Position:

• chr20-58909186-C-G

Variant summary

Our verdict is Likely pathogenic. Variant got 7 ACMG points: 7P and 0B. PM1 PM2 PP2 PP3_Moderate

The NM_000516.7(GNAS):​c.555C>G​(p.Ile185Met) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Synonymous variant affecting the same amino acid position (i.e. I185I) has been classified as Benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: GNAS NM_000516.7 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.27

Genes affected

GNAS (HGNC:4392): (GNAS complex locus) This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012]

GNAS (HGNC:):

ACMG classification

Verdict is Likely_pathogenic. Variant got 7 ACMG points.

• PM1: In a chain Neuroendocrine secretory protein 55 (size 198) in uniprot entity GNAS3_HUMAN there are 67 pathogenic changes around while only 1 benign (99%) in NM_000516.7
• PM2: Very rare variant in population databases, with high coverage
• PP2: Missense variant in gene, where missense usually causes diseases (based on misZ statistic), GNAS. . Gene score misZ 2.6546 (greater than the threshold 3.09). Trascript score misZ 4.8361 (greater than threshold 3.09). GenCC has associacion of gene with ACTH-independent macronodular adrenal hyperplasia 1, pseudohypoparathyroidism type 1B, pseudohypoparathyroidism type 1C, pseudohypoparathyroidism type 1A, progressive osseous heteroplasia, pseudopseudohypoparathyroidism, McCune-Albright syndrome.
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.882

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
GNAS	NM_000516.7	c.555C>G	p.Ile185Met	missense_variant	7/13	ENST00000371085.8	NP_000507.1
GNAS	NM_016592.5	c.*461C>G		3_prime_UTR_variant	7/13	ENST00000371075.7	NP_057676.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
GNAS	ENST00000371085.8	c.555C>G	p.Ile185Met	missense_variant	7/13	1	NM_000516.7	ENSP00000360126.3
GNAS	ENST00000676826.2	c.2487C>G	p.Ile829Met	missense_variant	7/13			ENSP00000504675.2
GNAS	ENST00000371102.8	c.2442C>G	p.Ile814Met	missense_variant	6/12	5		ENSP00000360143.4
GNAS	ENST00000354359.12	c.558C>G	p.Ile186Met	missense_variant	7/13	1		ENSP00000346328.7
GNAS	ENST00000371095.7	c.513C>G	p.Ile171Met	missense_variant	6/12	1		ENSP00000360136.3
GNAS	ENST00000470512.6	c.381C>G	p.Ile127Met	missense_variant	7/13	5		ENSP00000499552.2
GNAS	ENST00000480232.6	c.381C>G	p.Ile127Met	missense_variant	8/14	5		ENSP00000499545.2
GNAS	ENST00000663479.2	c.381C>G	p.Ile127Met	missense_variant	7/13			ENSP00000499353.2
GNAS	ENST00000462499.6	c.336C>G	p.Ile112Met	missense_variant	6/12	2		ENSP00000499758.2
GNAS	ENST00000467227.6	c.336C>G	p.Ile112Met	missense_variant	7/13	3		ENSP00000499681.2
GNAS	ENST00000478585.6	c.336C>G	p.Ile112Met	missense_variant	6/12	2		ENSP00000499762.2
GNAS	ENST00000481039.6	c.336C>G	p.Ile112Met	missense_variant	6/12	5		ENSP00000499767.2
GNAS	ENST00000485673.6	c.336C>G	p.Ile112Met	missense_variant	6/12	5		ENSP00000499334.2
GNAS	ENST00000488546.6	c.336C>G	p.Ile112Met	missense_variant	6/12	5		ENSP00000499332.2
GNAS	ENST00000492907.6	c.336C>G	p.Ile112Met	missense_variant	6/12	3		ENSP00000499443.2
GNAS	ENST00000371075.7	c.*461C>G		3_prime_UTR_variant	7/13	1	NM_016592.5	ENSP00000360115.3
GNAS	ENST00000453292.7	c.*416C>G		3_prime_UTR_variant	6/12	5		ENSP00000392000.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.65
BayesDel_addAF	Pathogenic	0.28	D
BayesDel_noAF	Pathogenic	0.16
CADD	Uncertain	26
DANN	Uncertain	1.0
DEOGEN2	Pathogenic	0.81	D;.;.;.;D;.;.
Eigen	Uncertain	0.44
Eigen_PC	Uncertain	0.40
FATHMM_MKL	Uncertain	0.93	D
LIST_S2	Uncertain	0.94	D;D;D;D;D;D;D
M_CAP	Pathogenic	0.94	D
MetaRNN	Pathogenic	0.88	D;D;D;D;D;D;D
MetaSVM	Pathogenic	1.1	D
MutationAssessor	Pathogenic	3.1	.;.;.;.;M;.;.
PrimateAI	Uncertain	0.70	T
PROVEAN	Benign	-2.2	N;N;.;N;N;N;N
REVEL	Pathogenic	0.82
Sift	Pathogenic	0.0	D;D;.;D;D;D;D
Sift4G	Uncertain	0.012	D;D;D;D;D;D;D
Polyphen		0.99	D;.;.;.;P;.;B
Vest4		0.53
MutPred		0.66		Gain of sheet (P = 0.0011);.;.;.;.;.;.;
MVP		0.98
MPC		3.1
ClinPred		0.99	D
GERP RS		4.0
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.88
gMVP		0.90

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: rs8620; hg19: chr20-57484241;