rs1555761983

Variant names:

Your query was ambiguous. Multiple possible variants found:

Variant summary

Our verdict is Uncertain significance. The variant received 4 ACMG points: 4P and 0B. PM1PM2

The NM_001387283.1(SMARCA4):c.1432A>G(p.Ser478Gly) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Uncertain significance (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. S478N) has been classified as Uncertain significance.

Frequency

Genomes: not found (cov: 31)

Consequence

SMARCA4
NM_001387283.1 missense

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 9.29

Publications

0 publications found

Variant links:

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 Gene-Disease associations (from GenCC):

Coffin-Siris syndrome
Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: ClinGen, Orphanet, Illumina
intellectual disability, autosomal dominant 16
Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: G2P, Labcorp Genetics (formerly Invitae), Ambry Genetics
rhabdoid tumor predisposition syndrome 2
Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Ambry Genetics, ClinGen, Genomics England PanelApp, Labcorp Genetics (formerly Invitae), G2P
uterine corpus sarcoma
Inheritance: AR Classification: MODERATE Submitted by: Genomics England PanelApp
familial rhabdoid tumor
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
hereditary nonpolyposis colon cancer
Inheritance: AD Classification: LIMITED Submitted by: ClinGen

SMARCA4 links:

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ACMG classification

Classification was made for transcript

Our verdict: Uncertain_significance. The variant received 4 ACMG points.

PM1

In a hotspot region, there are 2 aminoacids with missense pathogenic changes in the window of +-8 aminoacids around while only 1 benign, 15 uncertain in NM_001387283.1

PM2

Very rare variant in population databases, with high coverage;

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SMARCA4	NM_001387283.1 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 9 of 36	ENST00000646693.2	NP_001374212.1
SMARCA4	NM_003072.5 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 9 of 35	ENST00000344626.10	NP_003063.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein
SMARCA4	ENST00000646693.2 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 9 of 36		NM_001387283.1	ENSP00000495368.1
SMARCA4	ENST00000344626.10 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 9 of 35	1	NM_003072.5	ENSP00000343896.4
SMARCA4	ENST00000643549.1 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 9 of 35			ENSP00000493975.1
SMARCA4	ENST00000541122.6 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 10 of 35	5		ENSP00000445036.2
SMARCA4	ENST00000643296.1 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 9 of 34			ENSP00000496635.1
SMARCA4	ENST00000644737.1 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 9 of 34			ENSP00000495548.1
SMARCA4	ENST00000589677.5 link	c.1432A>G	p.Ser478Gly	missense_variant	Exon 10 of 35	5		ENSP00000464778.1
SMARCA4	ENST00000643995.1 link	c.844A>G	p.Ser282Gly	missense_variant	Exon 6 of 32			ENSP00000496004.1
SMARCA4	ENST00000644963.1 link	c.76A>G	p.Ser26Gly	missense_variant	Exon 2 of 28			ENSP00000495599.1
SMARCA4	ENST00000644065.1 link	c.160A>G	p.Ser54Gly	missense_variant	Exon 2 of 27			ENSP00000493615.1
SMARCA4	ENST00000642350.1 link	c.-81A>G		upstream_gene_variant				ENSP00000495355.1

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

Cov.:

GnomAD4 genome

Cov.:

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Pathogenic

0.65

BayesDel_addAF

Uncertain

0.019

BayesDel_noAF

Benign

-0.21

CADD

Uncertain

(source)

DANN

Uncertain

1.0

DEOGEN2

Uncertain

0.69

D;.;T;.;.;.;.;.;.;.;D;.;.;.;.;.;T;T

Eigen

Uncertain

0.54

Eigen_PC

Uncertain

0.56

FATHMM_MKL

Pathogenic

0.99

LIST_S2

Uncertain

0.97

.;D;.;.;.;.;D;.;.;.;D;.;D;D;D;D;D;D

M_CAP

Benign

0.085

MetaRNN

Uncertain

0.62

D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D

MetaSVM

Benign

-0.88

MutationAssessor

Benign

1.7

L;.;.;.;L;L;.;L;L;L;L;L;L;L;L;L;.;.

PhyloP100

9.3

PrimateAI

Pathogenic

0.87

PROVEAN

Uncertain

-2.7

D;.;.;.;.;.;.;.;.;.;D;.;D;.;D;.;D;D

REVEL

Uncertain

0.31

Sift

Benign

0.046

D;.;.;.;.;.;.;.;.;.;D;.;T;.;T;.;T;T

Sift4G

Benign

0.080

T;.;.;.;.;.;.;.;.;.;T;.;T;T;T;T;T;T

Polyphen

0.95

P;.;P;.;.;.;.;.;.;.;P;.;.;.;.;.;.;P

Vest4

0.57

MutPred

0.55

Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);Loss of disorder (P = 0.131);

MVP

0.66

MPC

2.2

ClinPred

0.97

GERP RS

4.5

PromoterAI

0.049

Neutral

(source)

Varity_R

0.49

gMVP

0.96

Mutation Taster

=25/75

disease causing

(source)

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Computational scores

Splicing

Publications

Other links and lift over