rs1321535007

Positions:

• chr19-11058811-C-A
• chr19-11058811-C-G
• chr19-11058811-C-T

Variant summary

Our verdict is Pathogenic. Variant got 10 ACMG points: 10P and 0B. PVS1 PM2

The NM_003072.5(SMARCA4):​c.4557C>A​(p.Tyr1519*) variant causes a stop gained 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. Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 32)
• Consequence: SMARCA4 NM_003072.5 stop_gained
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.40

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]

SMARCA4 (HGNC:):

ACMG classification

Verdict is Pathogenic. Variant got 10 ACMG points.

• PVS1: Loss of function variant, product undergoes nonsense mediated mRNA decay. LoF is a known mechanism of disease.
• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SMARCA4	NM_001387283.1	c.4653C>A	p.Tyr1551*	stop_gained	33/36	ENST00000646693.2	NP_001374212.1
SMARCA4	NM_003072.5	c.4557C>A	p.Tyr1519*	stop_gained	32/35	ENST00000344626.10	NP_003063.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SMARCA4	ENST00000646693.2	c.4653C>A	p.Tyr1551*	stop_gained	33/36		NM_001387283.1	ENSP00000495368.1
SMARCA4	ENST00000344626.10	c.4557C>A	p.Tyr1519*	stop_gained	32/35	1	NM_003072.5	ENSP00000343896.4
SMARCA4	ENST00000643549.1	c.4563C>A	p.Tyr1521*	stop_gained	32/35			ENSP00000493975.1
SMARCA4	ENST00000541122.6	c.4467C>A	p.Tyr1489*	stop_gained	32/35	5		ENSP00000445036.2
SMARCA4	ENST00000643296.1	c.4467C>A	p.Tyr1489*	stop_gained	31/34			ENSP00000496635.1
SMARCA4	ENST00000644737.1	c.4467C>A	p.Tyr1489*	stop_gained	31/34			ENSP00000495548.1
SMARCA4	ENST00000589677.5	c.4464C>A	p.Tyr1488*	stop_gained	32/35	5		ENSP00000464778.1
SMARCA4	ENST00000643995.1	c.3978C>A	p.Tyr1326*	stop_gained	29/32			ENSP00000496004.1
SMARCA4	ENST00000644963.1	c.3207C>A	p.Tyr1069*	stop_gained	25/28			ENSP00000495599.1
SMARCA4	ENST00000644065.1	c.3189C>A	p.Tyr1063*	stop_gained	24/27			ENSP00000493615.1
SMARCA4	ENST00000642350.1	c.3051C>A	p.Tyr1017*	stop_gained	24/27			ENSP00000495355.1
SMARCA4	ENST00000643857.1	c.2895+448C>A		intron_variant				ENSP00000494159.1
SMARCA4	ENST00000538456.4	c.699+448C>A		intron_variant		3		ENSP00000495197.1

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
BayesDel_addAF	Pathogenic	0.63	D
BayesDel_noAF	Pathogenic	0.54
CADD	Pathogenic	40
DANN	Uncertain	1.0
Eigen	Uncertain	0.62
Eigen_PC	Uncertain	0.46
FATHMM_MKL	Benign	0.58	D
Vest4		0.99
GERP RS		3.7
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7

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

No publications associated with this variant yet.

Other links and lift over

hg19: chr19-11169487;