rs864321679

Variant names:

• chr3-52563363-CCTCACTAT-C
• rs864321679
• NM_001405607.1:c.4043_4050delATAGTGAG

Variant summary

Our verdict is Uncertain significance. The variant received 3 ACMG points: 3P and 0B. PM2 PP5

The NM_001405607.1(PBRM1):​c.4043_4050delATAGTGAG​(p.Asp1348GlyfsTer3) variant causes a frameshift 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 Pathogenic (no stars). Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 31)
• Consequence: PBRM1 NM_001405607.1 frameshift
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 7.84
• Publications: 3 publications found

Genes affected

PBRM1 (HGNC:30064): (polybromo 1) This locus encodes a subunit of ATP-dependent chromatin-remodeling complexes. The encoded protein has been identified as in integral component of complexes necessary for ligand-dependent transcriptional activation by nuclear hormone receptors. Mutations at this locus have been associated with primary clear cell renal cell carcinoma. [provided by RefSeq, Feb 2012]

UQCC5 (HGNC:37257): (ubiquinol-cytochrome c reductase complex assembly factor 5) Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 3 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 3-52563363-CCTCACTAT-C is Pathogenic according to our data. Variant chr3-52563363-CCTCACTAT-C is described in ClinVar as Pathogenic. ClinVar VariationId is 218955.Status of the report is no_assertion_criteria_provided, 0 stars.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001405607.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PBRM1	NM_001405607.1	MANE Select	c.4043_4050delATAGTGAG	p.Asp1348GlyfsTer3	frameshift	Exon 26 of 32	NP_001392536.1
	PBRM1	NM_001405601.1		c.4043_4050delATAGTGAG	p.Asp1348GlyfsTer3	frameshift	Exon 26 of 32	NP_001392530.1
	PBRM1	NM_001405598.1		c.4025_4032delATAGTGAG	p.Asp1342GlyfsTer3	frameshift	Exon 25 of 31	NP_001392527.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PBRM1	ENST00000707071.1	MANE Select	c.4043_4050delATAGTGAG	p.Asp1348GlyfsTer3	frameshift	Exon 26 of 32	ENSP00000516722.1
	PBRM1	ENST00000296302.11	TSL:1	c.3998_4005delATAGTGAG	p.Asp1333GlyfsTer3	frameshift	Exon 24 of 30	ENSP00000296302.7
	PBRM1	ENST00000409114.7	TSL:1	c.4043_4050delATAGTGAG	p.Asp1348GlyfsTer3	frameshift	Exon 25 of 30	ENSP00000386643.3

Frequencies

GnomAD3 genomes Cov.: 31

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome Cov.: 31

ClinVar

ClinVar submissions as Germline

Significance: Pathogenic

Revision: no assertion criteria provided

Pathogenic	VUS	Benign	Condition
1	-	-	Clear cell carcinoma of kidney (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		7.8
Mutation Taster		=0/200	disease causing (ClinVar)

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs864321679; hg19: chr3-52597379;