19-57712730-C-T

Variant names:

• chr19-57712730-C-T
• rs4801516
• ENST00000594684.1:c.33+30486C>T

Variant summary

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

The ENST00000594684.1(ENSG00000269026):​c.33+30486C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.516 in 151,860 control chromosomes in the GnomAD database, including 20,538 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.52 (20538 hom., cov: 31)
• Consequence: ENSG00000269026 ENST00000594684.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.321
• Publications: 7 publications found

Genes affected

ENSG00000269026 (HGNC:):

ZNF551 (HGNC:25108): (zinc finger protein 551) 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]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.646 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000594684.1. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000269026	ENST00000594684.1	TSL:1	c.33+30486C>T		intron	N/A	ENSP00000472160.1	M0R1X1
	ZNF551	ENST00000596085.1	TSL:2	c.158-4437C>T		intron	N/A	ENSP00000472230.1	M0R209
	ENSG00000269026	ENST00000599221.1	TSL:3	n.200+30486C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.516 AC: 78311 AN: 151742 Hom.: 20501 Cov.: 31

Gnomad AFR AF: 0.550

Gnomad AMI AF: 0.597

Gnomad AMR AF: 0.548

Gnomad ASJ AF: 0.523

Gnomad EAS AF: 0.666

Gnomad SAS AF: 0.357

Gnomad FIN AF: 0.552

Gnomad MID AF: 0.509

Gnomad NFE AF: 0.481

Gnomad OTH AF: 0.530

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.516 AC: 78408 AN: 151860 Hom.: 20538 Cov.: 31 AF XY: 0.520 AC XY: 38569 AN XY: 74206

African (AFR) AF: 0.551 AC: 22805 AN: 41406

American (AMR) AF: 0.549 AC: 8375 AN: 15260

Ashkenazi Jewish (ASJ) AF: 0.523 AC: 1810 AN: 3464

East Asian (EAS) AF: 0.665 AC: 3424 AN: 5150

South Asian (SAS) AF: 0.357 AC: 1718 AN: 4808

European-Finnish (FIN) AF: 0.552 AC: 5810 AN: 10524

Middle Eastern (MID) AF: 0.514 AC: 151 AN: 294

European-Non Finnish (NFE) AF: 0.481 AC: 32649 AN: 67938

Other (OTH) AF: 0.533 AC: 1124 AN: 2108

Alfa AF: 0.486 Hom.: 13759

Bravo AF: 0.519

Asia WGS AF: 0.524 AC: 1821 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.81
DANN	Benign	0.58
PhyloP100		-0.32
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs4801516; hg19: chr19-58224098;