chr9-86301294-G-C

Variant names:

• chr9-86301294-G-C
• rs1213885128
• NM_024617.4:c.4402C>G

Variant summary

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

The NM_024617.4(TUT7):​c.4402C>G​(p.Gln1468Glu) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 12/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: TUT7 NM_024617.4 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 4.49

Genes affected

TUT7 (HGNC:25817): (terminal uridylyl transferase 7) Enables RNA uridylyltransferase activity and miRNA binding activity. Involved in RNA metabolic process and negative regulation of transposition, RNA-mediated. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

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=0.12501857).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TUT7	NM_024617.4	c.4402C>G	p.Gln1468Glu	missense_variant	Exon 26 of 27	ENST00000375963.8	NP_078893.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TUT7	ENST00000375963.8	c.4402C>G	p.Gln1468Glu	missense_variant	Exon 26 of 27	5	NM_024617.4	ENSP00000365130.3
TUT7	ENST00000375960.6	c.3694C>G	p.Gln1232Glu	missense_variant	Exon 19 of 20	1		ENSP00000365127.2
TUT7	ENST00000277141.10	c.2269C>G	p.Gln757Glu	missense_variant	Exon 27 of 28	2		ENSP00000277141.6
TUT7	ENST00000375957.5	c.1102C>G	p.Gln368Glu	missense_variant	Exon 11 of 12	2		ENSP00000365124.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD3 exomes AF: 0.00000400 AC: 1 AN: 250152 Hom.: 0 AF XY: 0.00000739 AC XY: 1 AN XY: 135330

Gnomad AFR exome AF: 0.00

Gnomad AMR exome AF: 0.00

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.00

Gnomad SAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.00000888

Gnomad OTH exome AF: 0.00

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

Dec 19, 2023

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The c.4402C>G (p.Q1468E) alteration is located in exon 26 (coding exon 25) of the ZCCHC6 gene. This alteration results from a C to G substitution at nucleotide position 4402, causing the glutamine (Q) at amino acid position 1468 to be replaced by a glutamic acid (E). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.13
BayesDel_addAF	Benign	-0.0048	T
BayesDel_noAF	Benign	-0.24
CADD	Uncertain	24
DANN	Uncertain	0.98
DEOGEN2	Benign	0.0040	.;.;T;T
Eigen	Benign	-0.0055
Eigen_PC	Benign	0.19
FATHMM_MKL	Uncertain	0.96	D
LIST_S2	Uncertain	0.89	D;D;D;D
M_CAP	Benign	0.019	T
MetaRNN	Benign	0.13	T;T;T;T
MetaSVM	Benign	-0.60	T
MutationAssessor	Benign	1.0	.;.;.;L
PrimateAI	Uncertain	0.52	T
PROVEAN	Benign	-0.13	N;N;N;N
REVEL	Benign	0.22
Sift	Benign	0.12	T;T;T;T
Sift4G	Benign	1.0	T;T;T;T
Polyphen		0.092, 0.14	.;B;.;B
Vest4		0.56
MutPred		0.29		.;.;.;Gain of ubiquitination at K1470 (P = 0.02);
MVP		0.093
MPC		1.4
ClinPred		0.38	T
GERP RS		5.2
Varity_R		0.10
gMVP		0.19

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

LitVar

Other links and lift over

dbSNP: rs1213885128; hg19: chr9-88916209;