NM_003072.5(SMARCA4):c.1812+11del AND Rhabdoid tumor predisposition syndrome 2

Germline classification:: Likely benign (1 submission)
Last evaluated:: May 27, 2022
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV002131874.6

Allele description [Variation Report for NM_003072.5(SMARCA4):c.1812+11del]

NM_003072.5(SMARCA4):c.1812+11del

Gene:

SMARCA4:SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

19p13.2

Genomic location:

Preferred name:

NM_003072.5(SMARCA4):c.1812+11del

HGVS:

NC_000019.10:g.10996555del
NG_011556.3:g.40624del
NM_001128844.3:c.1812+11del
NM_001128845.2:c.1812+11del
NM_001128846.2:c.1812+11del
NM_001128847.4:c.1812+11del
NM_001128848.2:c.1812+11del
NM_001128849.3:c.1812+11del
NM_001374457.1:c.1812+11del
NM_001387283.1:c.1812+11del
NM_003072.5:c.1812+11delMANE SELECT
LRG_878t1:c.1812+11del
LRG_878:g.40624del
NC_000019.9:g.11107231del
NG_011556.2:g.40634del

Links:

dbSNP: rs2145982263

NCBI 1000 Genomes Browser:

rs2145982263

Molecular consequence:

NM_001128844.3:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_001128845.2:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_001128846.2:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_001128847.4:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_001128848.2:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_001128849.3:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_001374457.1:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_001387283.1:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]
NM_003072.5:c.1812+11del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Rhabdoid tumor predisposition syndrome 2 (RTPS2)
Identifiers:: MONDO: MONDO:0013224; MedGen: C2750074; Orphanet: 231108; Orphanet: 69077; OMIM: 613325

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002454586	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (May 27, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002454586

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(May 27, 2022)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV002454586.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine