2-201316524-C-T

Position:

• chr2-201316524-C-T

Variant summary

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

The ENST00000392257.8(FLACC1):​c.676-7274G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.72 in 151,918 control chromosomes in the GnomAD database, including 39,783 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 0.72 (39783 hom., cov: 30)
• Consequence: FLACC1 ENST00000392257.8 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.00

Genes affected

FLACC1 (HGNC:14439): (flagellum associated containing coiled-coil domains 1) Predicted to be located in cytoplasmic vesicle and sperm flagellum. Predicted to be active in cytoplasm; outer dense fiber; and sperm fibrous sheath. [provided by Alliance of Genome Resources, Apr 2022]

CASP8 (HGNC:1509): (caspase 8) This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes composed of a prodomain, a large protease subunit, and a small protease subunit. Activation of caspases requires proteolytic processing at conserved internal aspartic residues to generate a heterodimeric enzyme consisting of the large and small subunits. This protein is involved in the programmed cell death induced by Fas and various apoptotic stimuli. The N-terminal FADD-like death effector domain of this protein suggests that it may interact with Fas-interacting protein FADD. This protein was detected in the insoluble fraction of the affected brain region from Huntington disease patients but not in those from normal controls, which implicated the role in neurodegenerative diseases. Many alternatively spliced transcript variants encoding different isoforms have been described, although not all variants have had their full-length sequences determined. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.807 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
FLACC1	NM_001127391.3	c.676-7274G>A		intron_variant		ENST00000392257.8	NP_001120863.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
FLACC1	ENST00000392257.8	c.676-7274G>A		intron_variant		1	NM_001127391.3	ENSP00000376086	P1

Frequencies

GnomAD3 genomes AF: 0.720 AC: 109361 AN: 151800 Hom.: 39744 Cov.: 30

Gnomad AFR AF: 0.786

Gnomad AMI AF: 0.766

Gnomad AMR AF: 0.577

Gnomad ASJ AF: 0.625

Gnomad EAS AF: 0.698

Gnomad SAS AF: 0.828

Gnomad FIN AF: 0.666

Gnomad MID AF: 0.706

Gnomad NFE AF: 0.721

Gnomad OTH AF: 0.677

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

GnomAD4 genome AF: 0.720 AC: 109447 AN: 151918 Hom.: 39783 Cov.: 30 AF XY: 0.717 AC XY: 53242 AN XY: 74250

Gnomad4 AFR AF: 0.786

Gnomad4 AMR AF: 0.576

Gnomad4 ASJ AF: 0.625

Gnomad4 EAS AF: 0.697

Gnomad4 SAS AF: 0.829

Gnomad4 FIN AF: 0.666

Gnomad4 NFE AF: 0.721

Gnomad4 OTH AF: 0.678

Alfa AF: 0.731 Hom.: 5027

Bravo AF: 0.713

Asia WGS AF: 0.788 AC: 2740 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.52
DANN	Benign	0.34

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: rs1830298; hg19: chr2-202181247;