ENST00000444991.6:c.479A>G

Variant names:

• chr19-36991249-A-G
• rs1667354
• ENST00000444991.6:c.479A>G
• ZNF568 p.Asp160Gly

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000444991.6(ZNF568):​c.479A>G​(p.Asp160Gly) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.539 in 1,534,716 control chromosomes in the GnomAD database, including 225,748 homozygotes. In-silico tool predicts a benign outcome for this variant. 10/16 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as (no stars).

• Frequency:
  • Genomes: 𝑓 0.56 (24509 hom., cov: 32)
  • Exomes 𝑓: 0.54 (201239 hom.)
• Consequence: ZNF568 ENST00000444991.6 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.316
• Publications: 24 publications found

Genes affected

ZNF568 (HGNC:25392): (zinc finger protein 568) 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 embryonic placenta morphogenesis and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ENSG00000291239 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (MetaRNN=8.637041E-6).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.666 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000444991.6. 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
	ZNF568	NM_001204838.2		c.479A>G	p.Asp160Gly	missense	Exon 8 of 10	NP_001191767.1	C9JLX5
	ZNF568	NM_001204839.2		c.287A>G	p.Asp96Gly	missense	Exon 7 of 9	NP_001191768.1	Q3ZCX4-3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZNF568	ENST00000444991.6	TSL:1	c.479A>G	p.Asp160Gly	missense	Exon 8 of 10	ENSP00000389794.2	C9JLX5
	ENSG00000291239	ENST00000706165.1		c.479A>G	p.Asp160Gly	missense	Exon 10 of 12	ENSP00000516244.1	C9JLX5
	ZNF568	ENST00000591887.1	TSL:1	n.197A>G		non_coding_transcript_exon	Exon 1 of 2

Frequencies

GnomAD3 genomes AF: 0.559 AC: 84876 AN: 151902 Hom.: 24471 Cov.: 32

Gnomad AFR AF: 0.673

Gnomad AMI AF: 0.265

Gnomad AMR AF: 0.536

Gnomad ASJ AF: 0.461

Gnomad EAS AF: 0.263

Gnomad SAS AF: 0.571

Gnomad FIN AF: 0.546

Gnomad MID AF: 0.545

Gnomad NFE AF: 0.527

Gnomad OTH AF: 0.552

GnomAD2 exomes AF: 0.510 AC: 70413 AN: 138030 AF XY: 0.514

Gnomad AFR exome AF: 0.673

Gnomad AMR exome AF: 0.487

Gnomad ASJ exome AF: 0.457

Gnomad EAS exome AF: 0.262

Gnomad FIN exome AF: 0.523

Gnomad NFE exome AF: 0.530

Gnomad OTH exome AF: 0.520

GnomAD4 exome AF: 0.537 AC: 741934 AN: 1382696 Hom.: 201239 Cov.: 40 AF XY: 0.537 AC XY: 366201 AN XY: 682232

African (AFR) AF: 0.676 AC: 21345 AN: 31558

American (AMR) AF: 0.498 AC: 17687 AN: 35492

Ashkenazi Jewish (ASJ) AF: 0.462 AC: 11627 AN: 25140

East Asian (EAS) AF: 0.289 AC: 10318 AN: 35706

South Asian (SAS) AF: 0.567 AC: 44799 AN: 78976

European-Finnish (FIN) AF: 0.530 AC: 18022 AN: 34028

Middle Eastern (MID) AF: 0.559 AC: 3186 AN: 5696

European-Non Finnish (NFE) AF: 0.542 AC: 584111 AN: 1078168

Other (OTH) AF: 0.532 AC: 30839 AN: 57932

GnomAD4 genome AF: 0.559 AC: 84975 AN: 152020 Hom.: 24509 Cov.: 32 AF XY: 0.558 AC XY: 41464 AN XY: 74310

African (AFR) AF: 0.673 AC: 27899 AN: 41454

American (AMR) AF: 0.536 AC: 8186 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.461 AC: 1598 AN: 3468

East Asian (EAS) AF: 0.264 AC: 1361 AN: 5164

South Asian (SAS) AF: 0.571 AC: 2744 AN: 4808

European-Finnish (FIN) AF: 0.546 AC: 5765 AN: 10550

Middle Eastern (MID) AF: 0.551 AC: 161 AN: 292

European-Non Finnish (NFE) AF: 0.527 AC: 35860 AN: 67982

Other (OTH) AF: 0.550 AC: 1159 AN: 2106

Alfa AF: 0.524 Hom.: 70805

Bravo AF: 0.560

Asia WGS AF: 0.468 AC: 1629 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.22
BayesDel_addAF	Benign	-0.64	T
BayesDel_noAF	Benign	-0.55
CADD	Benign	15
DANN	Uncertain	0.98
DEOGEN2	Benign	0.014	T
Eigen	Benign	-0.61
Eigen_PC	Benign	-0.60
FATHMM_MKL	Benign	0.066	N
LIST_S2	Benign	0.18	T
MetaRNN	Benign	0.0000086	T
MetaSVM	Benign	-1.0	T
PhyloP100		-0.32
PROVEAN	Benign	-2.2	N
REVEL	Benign	0.051
Sift	Benign	0.20	T
Sift4G	Benign	0.15	T
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs1667354;

hg19: chr19-37482151;

COSMIC: COSV71278669;

COSMIC: COSV71278669;