rs1291643997

Variant names:

• chr19-11027775-A-C
• rs1291643997
• NM_001387283.1:c.3216-9A>C

Your query was ambiguous. Multiple possible variants found:

• chr19-11027775-A-C
• chr19-11027775-A-T

Variant summary

Our verdict is Likely benign. Variant got -4 ACMG points: 2P and 6B. PM2 BP4_Strong BP6_Moderate

The NM_003072.5(SMARCA4):​c.3216-9A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000657 in 152,108 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

• Frequency: Genomes: 𝑓 0.0000066 (0 hom., cov: 33)
• Consequence: SMARCA4 NM_003072.5 intron
• Scores: Splicing: ADA: 0.00007973
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -5.10

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 Likely_benign. Variant got -4 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BP6: Variant 19-11027775-A-C is Benign according to our data. Variant chr19-11027775-A-C is described in ClinVar as [Likely_benign]. Clinvar id is 537906.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SMARCA4	NM_001387283.1	c.3216-9A>C		intron_variant	Intron 23 of 35	ENST00000646693.2	NP_001374212.1
SMARCA4	NM_003072.5	c.3216-9A>C		intron_variant	Intron 23 of 34	ENST00000344626.10	NP_003063.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SMARCA4	ENST00000646693.2	c.3216-9A>C		intron_variant	Intron 23 of 35		NM_001387283.1	ENSP00000495368.1
SMARCA4	ENST00000344626.10	c.3216-9A>C		intron_variant	Intron 23 of 34	1	NM_003072.5	ENSP00000343896.4
SMARCA4	ENST00000643549.1	c.3216-9A>C		intron_variant	Intron 23 of 34			ENSP00000493975.1
SMARCA4	ENST00000541122.6	c.3216-9A>C		intron_variant	Intron 24 of 34	5		ENSP00000445036.2
SMARCA4	ENST00000643296.1	c.3216-9A>C		intron_variant	Intron 23 of 33			ENSP00000496635.1
SMARCA4	ENST00000644737.1	c.3216-9A>C		intron_variant	Intron 23 of 33			ENSP00000495548.1
SMARCA4	ENST00000589677.5	c.3216-9A>C		intron_variant	Intron 24 of 34	5		ENSP00000464778.1
SMARCA4	ENST00000643995.1	c.2628-9A>C		intron_variant	Intron 20 of 31			ENSP00000496004.1
SMARCA4	ENST00000644963.1	c.1860-9A>C		intron_variant	Intron 16 of 27			ENSP00000495599.1
SMARCA4	ENST00000644065.1	c.1941-9A>C		intron_variant	Intron 16 of 26			ENSP00000493615.1
SMARCA4	ENST00000642350.1	c.1701-9A>C		intron_variant	Intron 15 of 26			ENSP00000495355.1
SMARCA4	ENST00000643857.1	c.1569-9A>C		intron_variant	Intron 14 of 24			ENSP00000494159.1

Frequencies

GnomAD3 genomes AF: 0.00000657 AC: 1 AN: 152108 Hom.: 0 Cov.: 33

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0000147

Gnomad OTH AF: 0.00

GnomAD4 exome Cov.: 32

GnomAD4 genome AF: 0.00000657 AC: 1 AN: 152108 Hom.: 0 Cov.: 33 AF XY: 0.00 AC XY: 0 AN XY: 74308

Gnomad4 AFR AF: 0.00

Gnomad4 AMR AF: 0.00

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.00

Gnomad4 NFE AF: 0.0000147

Gnomad4 OTH AF: 0.00

Bravo AF: 0.00000378

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Rhabdoid tumor predisposition syndrome 2 Benign:1

Sep 17, 2017

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	0.0020
DANN	Benign	0.56

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Benign	0.000080
dbscSNV1_RF	Benign	0.042
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: rs1291643997; hg19: chr19-11138451;