rs1555773235

Variant names:

• chr19-11010389-A-G
• rs1555773235
• NM_001387283.1:c.2132A>G

Your query was ambiguous. Multiple possible variants found:

• chr19-11010389-A-G
• chr19-11010389-A-T

Variant summary

Our verdict is Uncertain significance. Variant got 2 ACMG points: 3P and 1B. PM2 PP2 BP4

The NM_003072.5(SMARCA4):​c.2132A>G​(p.Lys711Arg) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★★).

• Frequency: Genomes: not found (cov: 31)
• Consequence: SMARCA4 NM_003072.5 missense
• Clinical Significance: Uncertain significance criteria provided, multiple submitters, no conflicts U:3
• Conservation: PhyloP100: 6.42

Genes affected

SMARCA4 (HGNC:11100): (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4) The protein encoded by this gene is a member of the SWI/SNF family of proteins and is similar to the brahma protein of Drosophila. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. In addition, this protein can bind BRCA1, as well as regulate the expression of the tumorigenic protein CD44. Mutations in this gene cause rhabdoid tumor predisposition syndrome type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]

ACMG classification

Verdict is Uncertain_significance. Variant got 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP2: Missense variant in the SMARCA4 gene, where missense mutations are typically associated with disease (based on misZ statistic). The gene has 59 curated pathogenic missense variants (we use a threshold of 10). The gene has 56 curated benign missense variants. Gene score misZ: 6.8459 (above the threshold of 3.09). Trascript score misZ: 8.7957 (above the threshold of 3.09). GenCC associations: The gene is linked to uterine corpus sarcoma, Coffin-Siris syndrome 1, intellectual disability, autosomal dominant 16, rhabdoid tumor predisposition syndrome 2, familial rhabdoid tumor, hereditary nonpolyposis colon cancer, Coffin-Siris syndrome.
• BP4: Computational evidence support a benign effect (MetaRNN=0.29306424).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SMARCA4	NM_001387283.1	c.2132A>G	p.Lys711Arg	missense_variant	Exon 15 of 36	ENST00000646693.2	NP_001374212.1
SMARCA4	NM_003072.5	c.2132A>G	p.Lys711Arg	missense_variant	Exon 15 of 35	ENST00000344626.10	NP_003063.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SMARCA4	ENST00000646693.2	c.2132A>G	p.Lys711Arg	missense_variant	Exon 15 of 36		NM_001387283.1	ENSP00000495368.1
SMARCA4	ENST00000344626.10	c.2132A>G	p.Lys711Arg	missense_variant	Exon 15 of 35	1	NM_003072.5	ENSP00000343896.4
SMARCA4	ENST00000643549.1	c.2132A>G	p.Lys711Arg	missense_variant	Exon 15 of 35			ENSP00000493975.1
SMARCA4	ENST00000541122.6	c.2132A>G	p.Lys711Arg	missense_variant	Exon 16 of 35	5		ENSP00000445036.2
SMARCA4	ENST00000643296.1	c.2132A>G	p.Lys711Arg	missense_variant	Exon 15 of 34			ENSP00000496635.1
SMARCA4	ENST00000644737.1	c.2132A>G	p.Lys711Arg	missense_variant	Exon 15 of 34			ENSP00000495548.1
SMARCA4	ENST00000589677.5	c.2132A>G	p.Lys711Arg	missense_variant	Exon 16 of 35	5		ENSP00000464778.1
SMARCA4	ENST00000643995.1	c.1544A>G	p.Lys515Arg	missense_variant	Exon 12 of 32			ENSP00000496004.1
SMARCA4	ENST00000644963.1	c.776A>G	p.Lys259Arg	missense_variant	Exon 8 of 28			ENSP00000495599.1
SMARCA4	ENST00000644065.1	c.857A>G	p.Lys286Arg	missense_variant	Exon 8 of 27			ENSP00000493615.1
SMARCA4	ENST00000642350.1	c.617A>G	p.Lys206Arg	missense_variant	Exon 7 of 27			ENSP00000495355.1
SMARCA4	ENST00000643857.1	c.485A>G	p.Lys162Arg	missense_variant	Exon 6 of 25			ENSP00000494159.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 31

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:3

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

Intellectual disability, autosomal dominant 16 Uncertain:1

Jul 15, 2021

Genome-Nilou Lab

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Rhabdoid tumor predisposition syndrome 2 Uncertain:1

Sep 17, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This sequence change replaces lysine, which is basic and polar, with arginine, which is basic and polar, at codon 711 of the SMARCA4 protein (p.Lys711Arg). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with SMARCA4-related conditions. ClinVar contains an entry for this variant (Variation ID: 470287). Invitae Evidence Modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) indicates that this missense variant is not expected to disrupt SMARCA4 protein function with a negative predictive value of 95%. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. -

Hereditary cancer-predisposing syndrome Uncertain:1

Sep 04, 2024

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The p.K711R variant (also known as c.2132A>G), located in coding exon 14 of the SMARCA4 gene, results from an A to G substitution at nucleotide position 2132. The lysine at codon 711 is replaced by arginine, an amino acid with highly similar properties. Missense and in-frame variants in SMARCA4 are known to cause neurodevelopmental disorders; however, such associations with rhabdoid tumor predisposition syndrome including small cell carcinoma of the ovary-hypercalcemic type (SCCOHT) are exceedingly rare (Kosho T et al. Am J Med Genet C Semin Med Genet. 2014 Sep;166C(3):262-75; Jelinic P et al. Nat Genet. 2014 May;46(5):424-6). This amino acid position is well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Based on the supporting evidence, the association of this alteration with Coffin-Siris syndrome is unknown; however, the association of this alteration with rhabdoid tumor predisposition syndrome is unlikely. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.15
BayesDel_addAF	Uncertain	0.014	T
BayesDel_noAF	Benign	-0.22
CADD	Uncertain	25
DANN	Uncertain	0.99
DEOGEN2	Benign	0.32	T;.;T;.;.;.;.;.;.;.;T;.;.;.;.;.;T;T;.;.;.
Eigen	Benign	-0.22
Eigen_PC	Benign	-0.035
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Uncertain	0.95	.;D;.;.;.;.;D;.;.;.;D;.;D;D;D;D;D;D;D;D;D
M_CAP	Uncertain	0.13	D
MetaRNN	Benign	0.29	T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T
MetaSVM	Benign	-0.52	T
MutationAssessor	Benign	1.4	L;.;.;.;L;L;.;L;L;L;L;L;L;L;L;L;.;.;.;.;.
PrimateAI	Pathogenic	0.80	D
PROVEAN	Benign	-1.3	N;.;.;.;.;.;.;.;.;.;N;.;N;.;N;.;.;N;.;.;.
REVEL	Benign	0.24
Sift	Benign	0.34	T;.;.;.;.;.;.;.;.;.;T;.;T;.;T;.;.;T;.;.;.
Sift4G	Benign	0.33	T;.;.;.;.;.;.;.;.;.;T;.;T;T;T;T;T;T;.;.;.
Polyphen		0.0020	B;.;B;.;.;.;.;.;.;.;B;.;.;.;.;.;.;B;.;.;.
Vest4		0.26
MutPred		0.38		Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);Loss of ubiquitination at K711 (P = 0.0041);.;Loss of ubiquitination at K711 (P = 0.0041);.;.;.;
MVP		0.75
MPC		1.1
ClinPred		0.83	D
GERP RS		4.9
Varity_R		0.052
gMVP		0.53

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: rs1555773235; hg19: chr19-11121065;