rs6592508

chr11-73073628-A-Gchr11-73073628-A-T

Variant summary

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

The NM_014824.3(FCHSD2):c.165+10067T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.454 in 151,988 control chromosomes in the GnomAD database, including 16,598 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 0.45 (16598 hom., cov: 32)
• Consequence: FCHSD2 NM_014824.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.280

Genes affected

FCHSD2 (HGNC:29114): (FCH and double SH3 domains 2) Enables phosphatidylinositol-3,4,5-trisphosphate binding activity and phosphatidylinositol-3,4-bisphosphate binding activity. Involved in clathrin-dependent endocytosis and positive regulation of Arp2/3 complex-mediated actin nucleation. Located in plasma membrane. Colocalizes with clathrin-coated pit. [provided by Alliance of Genome Resources, Apr 2022]

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 (SAS) allele frequency at 95% confidence interval = 0.631 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FCHSD2	NM_014824.3	c.165+10067T>C		intron_variant		ENST00000409418.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FCHSD2	ENST00000409418.9	c.165+10067T>C		intron_variant		2	NM_014824.3	P1

Frequencies

GnomAD3 genomes AF: 0.454 AC: 68972 AN: 151870 Hom.: 16589 Cov.: 32

Gnomad AFR AF: 0.323

Gnomad AMI AF: 0.473

Gnomad AMR AF: 0.488

Gnomad ASJ AF: 0.378

Gnomad EAS AF: 0.618

Gnomad SAS AF: 0.651

Gnomad FIN AF: 0.654

Gnomad MID AF: 0.288

Gnomad NFE AF: 0.474

Gnomad OTH AF: 0.419

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

GnomAD4 genome AF: 0.454 AC: 68985 AN: 151988 Hom.: 16598 Cov.: 32 AF XY: 0.466 AC XY: 34651 AN XY: 74286

Gnomad4 AFR AF: 0.323

Gnomad4 AMR AF: 0.488

Gnomad4 ASJ AF: 0.378

Gnomad4 EAS AF: 0.619

Gnomad4 SAS AF: 0.650

Gnomad4 FIN AF: 0.654

Gnomad4 NFE AF: 0.474

Gnomad4 OTH AF: 0.417

Alfa AF: 0.475 Hom.: 9075

Bravo AF: 0.432

Asia WGS AF: 0.578 AC: 2003 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
Cadd	Benign	3.4
Dann	Benign	0.46

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: rs6592508; hg19: chr11-72784673;