rs3757949

chr8-11757489-G-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_001308093.3(GATA4):c.1149+406G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.314 in 152,172 control chromosomes in the GnomAD database, including 8,085 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.31 (8085 hom., cov: 34)
• Consequence: GATA4 NM_001308093.3 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.652

Genes affected

GATA4 (HGNC:4173): (GATA binding protein 4) This gene encodes a member of the GATA family of zinc-finger transcription factors. Members of this family recognize the GATA motif which is present in the promoters of many genes. This protein is thought to regulate genes involved in embryogenesis and in myocardial differentiation and function, and is necessary for normal testicular development. Mutations in this gene have been associated with cardiac septal defects. Additionally, alterations in gene expression have been associated with several cancer types. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BP6: Variant 8-11757489-G-C is Benign according to our data. Variant chr8-11757489-G-C is described in ClinVar as [Benign]. Clinvar id is 1241748.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.471 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
GATA4	NM_001308093.3	c.1149+406G>C		intron_variant		ENST00000532059.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
GATA4	ENST00000532059.6	c.1149+406G>C		intron_variant		1	NM_001308093.3	A1

Frequencies

GnomAD3 genomes AF: 0.314 AC: 47689 AN: 152054 Hom.: 8073 Cov.: 34

Gnomad AFR AF: 0.424

Gnomad AMI AF: 0.127

Gnomad AMR AF: 0.258

Gnomad ASJ AF: 0.292

Gnomad EAS AF: 0.487

Gnomad SAS AF: 0.357

Gnomad FIN AF: 0.313

Gnomad MID AF: 0.320

Gnomad NFE AF: 0.248

Gnomad OTH AF: 0.285

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

GnomAD4 genome AF: 0.314 AC: 47737 AN: 152172 Hom.: 8085 Cov.: 34 AF XY: 0.319 AC XY: 23695 AN XY: 74390

Gnomad4 AFR AF: 0.424

Gnomad4 AMR AF: 0.258

Gnomad4 ASJ AF: 0.292

Gnomad4 EAS AF: 0.487

Gnomad4 SAS AF: 0.355

Gnomad4 FIN AF: 0.313

Gnomad4 NFE AF: 0.248

Gnomad4 OTH AF: 0.284

Alfa AF: 0.296 Hom.: 854

Bravo AF: 0.310

Asia WGS AF: 0.430 AC: 1494 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

May 12, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
Cadd	Benign	2.0
Dann	Benign	0.22

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		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: rs3757949; hg19: chr8-11614998;