rs796230948

Variant names:

• chr10-124989638-G-C
• NM_022802.3:c.2838C>G

Your query was ambiguous. Multiple possible variants found:

• chr10-124989638-G-C
• chr10-124989638-G-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_022802.3(CTBP2):​c.2838C>G​(p.Ile946Met) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000686 in 1,457,744 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 13/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 31)
  • Exomes 𝑓: 6.9e-7 (0 hom.)
• Consequence: CTBP2 NM_022802.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.98

Genes affected

CTBP2 (HGNC:2495): (C-terminal binding protein 2) This gene produces alternative transcripts encoding two distinct proteins. One protein is a transcriptional repressor, while the other isoform is a major component of specialized synapses known as synaptic ribbons. Both proteins contain a NAD+ binding domain similar to NAD+-dependent 2-hydroxyacid dehydrogenases. A portion of the 3' untranslated region was used to map this gene to chromosome 21q21.3; however, it was noted that similar loci elsewhere in the genome are likely. Blast analysis shows that this gene is present on chromosome 10. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Feb 2014]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.18042228).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CTBP2	NM_022802.3	c.2838C>G	p.Ile946Met	missense_variant	Exon 9 of 9	ENST00000309035.11	NP_073713.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CTBP2	ENST00000309035.11	c.2838C>G	p.Ile946Met	missense_variant	Exon 9 of 9	1	NM_022802.3	ENSP00000311825.6
CTBP2	ENST00000337195.10	c.1218C>G	p.Ile406Met	missense_variant	Exon 11 of 11	1		ENSP00000338615.5

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome AF: 6.86e-7 AC: 1 AN: 1457744 Hom.: 0 Cov.: 30 AF XY: 0.00 AC XY: 0 AN XY: 724696

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 9.01e-7

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.070
BayesDel_addAF	Uncertain	0.087	D
BayesDel_noAF	Benign	-0.11
CADD	Benign	20
DANN	Benign	0.95
DEOGEN2	Benign	0.13	T;.;.;T;T;T
Eigen	Benign	-0.24
Eigen_PC	Benign	-0.058
FATHMM_MKL	Benign	0.68	D
LIST_S2	Uncertain	0.87	.;D;D;.;.;D
M_CAP	Benign	0.022	T
MetaRNN	Benign	0.18	T;T;T;T;T;T
MetaSVM	Benign	-0.52	T
MutationAssessor	Benign	0.76	N;.;.;N;N;N
PrimateAI	Uncertain	0.69	T
PROVEAN	Benign	-0.48	N;N;N;N;N;N
REVEL	Uncertain	0.34
Sift	Benign	0.11	T;T;T;T;T;T
Sift4G	Benign	0.39	T;T;T;T;T;T
Polyphen		0.0020	B;B;.;B;B;B
Vest4		0.19
MutPred		0.24		.;.;Gain of disorder (P = 0.0414);.;.;.;
MVP		0.84
MPC		2.0
ClinPred		0.60	D
GERP RS		3.2
Varity_R		0.12
gMVP		0.48

Splicing

Name	Calibrated prediction	Score	Prediction
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

No publications associated with this variant yet.

Other links and lift over

hg19: chr10-126678207;