13-48360118-G-C

Position:

• chr13-48360118-G-C

Variant summary

Our verdict is Uncertain significance. Variant got 4 ACMG points: 4P and 0B. PM1 PM2

The ENST00000267163.6(RB1):​c.709G>C​(p.Glu237Gln) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: RB1 ENST00000267163.6 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 7.18

Genes affected

RB1 (HGNC:9884): (RB transcriptional corepressor 1) The protein encoded by this gene is a negative regulator of the cell cycle and was the first tumor suppressor gene found. The encoded protein also stabilizes constitutive heterochromatin to maintain the overall chromatin structure. The active, hypophosphorylated form of the protein binds transcription factor E2F1. Defects in this gene are a cause of childhood cancer retinoblastoma (RB), bladder cancer, and osteogenic sarcoma. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 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 3 benign, 16 uncertain in ENST00000267163.6
• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RB1	NM_000321.3	c.709G>C	p.Glu237Gln	missense_variant	7/27	ENST00000267163.6	NP_000312.2
RB1	NM_001407165.1	c.709G>C	p.Glu237Gln	missense_variant	7/27		NP_001394094.1
RB1	NM_001407166.1	c.709G>C	p.Glu237Gln	missense_variant	7/17		NP_001394095.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RB1	ENST00000267163.6	c.709G>C	p.Glu237Gln	missense_variant	7/27	1	NM_000321.3	ENSP00000267163	P1
RB1	ENST00000467505.5	c.*77G>C		3_prime_UTR_variant, NMD_transcript_variant	2/3	1		ENSP00000434702
RB1	ENST00000650461.1	c.709G>C	p.Glu237Gln	missense_variant	7/27			ENSP00000497193
RB1	ENST00000525036.1	n.871G>C		non_coding_transcript_exon_variant	7/7	3

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
AlphaMissense	Benign	0.25
BayesDel_addAF	Uncertain	0.13	D
BayesDel_noAF	Uncertain	-0.040
CADD	Benign	22
DANN	Uncertain	0.99
DEOGEN2	Benign	0.40	T;.
Eigen	Uncertain	0.27
Eigen_PC	Uncertain	0.41
FATHMM_MKL	Uncertain	0.96	D
LIST_S2	Benign	0.85	D;D
M_CAP	Benign	0.026	D
MetaRNN	Uncertain	0.47	T;T
MetaSVM	Uncertain	0.31	D
MutationAssessor	Benign	1.9	L;.
MutationTaster	Benign	1.0	D
PrimateAI	Uncertain	0.60	T
PROVEAN	Benign	-0.85	N;.
REVEL	Uncertain	0.40
Sift	Benign	0.25	T;.
Sift4G	Benign	0.20	T;.
Polyphen		0.22	B;.
Vest4		0.53
MutPred		0.46		Gain of catalytic residue at K240 (P = 0.0019);Gain of catalytic residue at K240 (P = 0.0019);
MVP		0.82
MPC		0.94
ClinPred		0.85	D
GERP RS		5.6
Varity_R		0.27
gMVP		0.34

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.020		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: chr13-48934254;