chr19-52572269-G-A

Position:

• chr19-52572269-G-A

Variant summary

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

The NM_001172655.1(ZNF701):​c.28G>A​(p.Gly10Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 13/20 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: 33)
• Consequence: ZNF701 NM_001172655.1 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 0.252

Genes affected

ZNF701 (HGNC:25597): (zinc finger protein 701) Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ZNF701 (HGNC:):

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=0.16918409).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ZNF701	NM_018260.3	c.-71-1808G>A		intron_variant		ENST00000391785.8	NP_060730.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ZNF701	ENST00000391785.8	c.-71-1808G>A		intron_variant		1	NM_018260.3	ENSP00000375662.2

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 6

GnomAD4 genome Cov.: 33

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Ambry Genetics

Nov 13, 2024

The c.28G>A (p.G10S) alteration is located in exon 2 (coding exon 1) of the ZNF701 gene. This alteration results from a G to A substitution at nucleotide position 28, causing the glycine (G) at amino acid position 10 to be replaced by a serine (S). 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	0.088
BayesDel_addAF	Benign	-0.29	T
BayesDel_noAF	Benign	-0.66
CADD	Benign	4.5
DANN	Uncertain	0.99
DEOGEN2	Benign	0.0047	T;.;T
Eigen	Benign	-0.62
Eigen_PC	Benign	-0.92
FATHMM_MKL	Benign	0.0040	N
LIST_S2	Benign	0.79	.;T;T
M_CAP	Benign	0.0022	T
MetaRNN	Benign	0.17	T;T;T
MetaSVM	Benign	-0.99	T
PrimateAI	Benign	0.46	T
PROVEAN	Benign	-0.53	N;.;N
REVEL	Benign	0.056
Sift	Pathogenic	0.0	D;.;D
Sift4G	Benign	0.65	T;T;T
Vest4		0.26
MutPred		0.31		Gain of phosphorylation at G10 (P = 0.075);Gain of phosphorylation at G10 (P = 0.075);Gain of phosphorylation at G10 (P = 0.075);
MVP		0.12
MPC		0.48
ClinPred		0.41	T
GERP RS		0.16
Varity_R		0.16
gMVP		0.048

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: rs1423732625; hg19: chr19-53075522;