rs9513097

Variant names:

• chr13-28402252-C-T
• rs9513097
• NM_002019.4:c.1551+3528G>A

Variant summary

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

The NM_002019.4(FLT1):​c.1551+3528G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.28 in 152,034 control chromosomes in the GnomAD database, including 6,283 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 0.28 (6283 hom., cov: 32)
• Consequence: FLT1 NM_002019.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0200
• Publications: 8 publications found

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

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.427 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FLT1	NM_002019.4	c.1551+3528G>A		intron_variant	Intron 11 of 29	ENST00000282397.9	NP_002010.2
FLT1	NM_001160030.2	c.1551+3528G>A		intron_variant	Intron 11 of 14		NP_001153502.1
FLT1	NM_001159920.2	c.1551+3528G>A		intron_variant	Intron 11 of 12		NP_001153392.1
FLT1	NM_001160031.1	c.1552-3134G>A		intron_variant	Intron 11 of 11		NP_001153503.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FLT1	ENST00000282397.9	c.1551+3528G>A		intron_variant	Intron 11 of 29	1	NM_002019.4	ENSP00000282397.4

Frequencies

GnomAD3 genomes AF: 0.280 AC: 42527 AN: 151916 Hom.: 6281 Cov.: 32

Gnomad AFR AF: 0.217

Gnomad AMI AF: 0.291

Gnomad AMR AF: 0.217

Gnomad ASJ AF: 0.291

Gnomad EAS AF: 0.443

Gnomad SAS AF: 0.299

Gnomad FIN AF: 0.397

Gnomad MID AF: 0.209

Gnomad NFE AF: 0.300

Gnomad OTH AF: 0.269

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

GnomAD4 genome AF: 0.280 AC: 42545 AN: 152034 Hom.: 6283 Cov.: 32 AF XY: 0.282 AC XY: 20943 AN XY: 74272

African (AFR) AF: 0.217 AC: 8995 AN: 41470

American (AMR) AF: 0.216 AC: 3306 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.291 AC: 1011 AN: 3472

East Asian (EAS) AF: 0.442 AC: 2286 AN: 5170

South Asian (SAS) AF: 0.300 AC: 1445 AN: 4820

European-Finnish (FIN) AF: 0.397 AC: 4188 AN: 10538

Middle Eastern (MID) AF: 0.228 AC: 67 AN: 294

European-Non Finnish (NFE) AF: 0.300 AC: 20405 AN: 67974

Other (OTH) AF: 0.273 AC: 577 AN: 2114

Alfa AF: 0.288 Hom.: 807

Bravo AF: 0.263

Asia WGS AF: 0.359 AC: 1248 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	7.5
DANN	Benign	0.67
PhyloP100		0.020
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: rs9513097; hg19: chr13-28976389; COSMIC: COSV56740632;