chr13-28320932-A-G

Position:

• chr13-28320932-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_002019.4(FLT1):​c.3174+531T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.796 in 151,946 control chromosomes in the GnomAD database, including 48,934 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 0.80 (48934 hom., cov: 30)
• Consequence: FLT1 NM_002019.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0380

Genes affected

FLT1 (HGNC:3763): (fms related receptor tyrosine kinase 1) This gene encodes a member of the vascular endothelial growth factor receptor (VEGFR) family. VEGFR family members are receptor tyrosine kinases (RTKs) which contain an extracellular ligand-binding region with seven immunoglobulin (Ig)-like domains, a transmembrane segment, and a tyrosine kinase (TK) domain within the cytoplasmic domain. This protein binds to VEGFR-A, VEGFR-B and placental growth factor and plays an important role in angiogenesis and vasculogenesis. Expression of this receptor is found in vascular endothelial cells, placental trophoblast cells and peripheral blood monocytes. Multiple transcript variants encoding different isoforms have been found for this gene. Isoforms include a full-length transmembrane receptor isoform and shortened, soluble isoforms. The soluble isoforms are associated with the onset of pre-eclampsia.[provided by RefSeq, May 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.864 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
FLT1	NM_002019.4	c.3174+531T>C		intron_variant		ENST00000282397.9	NP_002010.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
FLT1	ENST00000282397.9	c.3174+531T>C		intron_variant		1	NM_002019.4	ENSP00000282397.4

Frequencies

GnomAD3 genomes AF: 0.796 AC: 120844 AN: 151828 Hom.: 48896 Cov.: 30

Gnomad AFR AF: 0.639

Gnomad AMI AF: 0.826

Gnomad AMR AF: 0.806

Gnomad ASJ AF: 0.885

Gnomad EAS AF: 0.882

Gnomad SAS AF: 0.834

Gnomad FIN AF: 0.825

Gnomad MID AF: 0.763

Gnomad NFE AF: 0.870

Gnomad OTH AF: 0.810

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

GnomAD4 genome AF: 0.796 AC: 120938 AN: 151946 Hom.: 48934 Cov.: 30 AF XY: 0.794 AC XY: 58995 AN XY: 74296

Gnomad4 AFR AF: 0.639

Gnomad4 AMR AF: 0.807

Gnomad4 ASJ AF: 0.885

Gnomad4 EAS AF: 0.882

Gnomad4 SAS AF: 0.834

Gnomad4 FIN AF: 0.825

Gnomad4 NFE AF: 0.870

Gnomad4 OTH AF: 0.812

Alfa AF: 0.839 Hom.: 14881

Bravo AF: 0.786

Asia WGS AF: 0.846 AC: 2941 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	3.2
DANN	Benign	0.56

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: rs9508016; hg19: chr13-28895069;