chr3-128485843-T-A

Position:

• chr3-128485843-T-A

Variant summary

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

The NM_032638.5(GATA2):​c.755A>T​(p.Tyr252Phe) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. Y252C) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: GATA2 NM_032638.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 7.96

Genes affected

GATA2 (HGNC:4171): (GATA binding protein 2) This gene encodes a member of the GATA family of zinc-finger transcription factors that are named for the consensus nucleotide sequence they bind in the promoter regions of target genes. The encoded protein plays an essential role in regulating transcription of genes involved in the development and proliferation of hematopoietic and endocrine cell lineages. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009]

ACMG classification

Verdict is Uncertain_significance. Variant got 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
GATA2	NM_001145661.2	c.755A>T	p.Tyr252Phe	missense_variant	4/7	ENST00000487848.6
GATA2	NM_032638.5	c.755A>T	p.Tyr252Phe	missense_variant	3/6	ENST00000341105.7
GATA2	NM_001145662.1	c.755A>T	p.Tyr252Phe	missense_variant	3/6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
GATA2	ENST00000341105.7	c.755A>T	p.Tyr252Phe	missense_variant	3/6	1	NM_032638.5	P1
GATA2	ENST00000487848.6	c.755A>T	p.Tyr252Phe	missense_variant	4/7	1	NM_001145661.2	P1
GATA2	ENST00000430265.6	c.755A>T	p.Tyr252Phe	missense_variant	3/6	1
GATA2	ENST00000696466.1	c.1037A>T	p.Tyr346Phe	missense_variant	5/8

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.13
BayesDel_addAF	Pathogenic	0.23	D
BayesDel_noAF	Uncertain	0.090
CADD	Benign	23
DANN	Uncertain	0.99
DEOGEN2	Pathogenic	0.80	D;.;D
Eigen	Uncertain	0.38
Eigen_PC	Uncertain	0.37
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Benign	0.84	.;T;T
M_CAP	Pathogenic	0.66	D
MetaRNN	Uncertain	0.47	T;T;T
MetaSVM	Pathogenic	1.1	D
MutationAssessor	Benign	1.9	L;L;L
MutationTaster	Benign	1.0	D;D;D
PrimateAI	Uncertain	0.76	T
PROVEAN	Uncertain	-3.0	D;D;D
REVEL	Pathogenic	0.75
Sift	Uncertain	0.0040	D;D;D
Sift4G	Uncertain	0.055	T;T;T
Polyphen		0.11	B;D;B
Vest4		0.44
MutPred		0.31		Gain of glycosylation at Y252 (P = 0.0115);Gain of glycosylation at Y252 (P = 0.0115);Gain of glycosylation at Y252 (P = 0.0115);
MVP		0.86
MPC		1.4
ClinPred		0.97	D
GERP RS		4.6
Varity_R		0.46
gMVP		0.55

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs1060500090; hg19: chr3-128204686; COSMIC: COSV62006225; COSMIC: COSV62006225;