rs3852402

chr9-95261655-C-Achr9-95261655-C-T

Variant summary

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

The NM_000136.3(FANCC):c.-78-12286G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.386 in 152,030 control chromosomes in the GnomAD database, including 11,934 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 0.39 (11934 hom., cov: 33)
• Consequence: FANCC NM_000136.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.54

Genes affected

FANCC (HGNC:3584): (FA complementation group C) The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group C. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.567 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FANCC	NM_000136.3	c.-78-12286G>T		intron_variant		ENST00000289081.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FANCC	ENST00000289081.8	c.-78-12286G>T		intron_variant		1	NM_000136.3	P1

Frequencies

GnomAD3 genomes AF: 0.386 AC: 58694 AN: 151910 Hom.: 11929 Cov.: 33

Gnomad AFR AF: 0.251

Gnomad AMI AF: 0.471

Gnomad AMR AF: 0.481

Gnomad ASJ AF: 0.353

Gnomad EAS AF: 0.586

Gnomad SAS AF: 0.453

Gnomad FIN AF: 0.471

Gnomad MID AF: 0.399

Gnomad NFE AF: 0.414

Gnomad OTH AF: 0.404

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

GnomAD4 genome AF: 0.386 AC: 58710 AN: 152030 Hom.: 11934 Cov.: 33 AF XY: 0.392 AC XY: 29126 AN XY: 74312

Gnomad4 AFR AF: 0.251

Gnomad4 AMR AF: 0.482

Gnomad4 ASJ AF: 0.353

Gnomad4 EAS AF: 0.584

Gnomad4 SAS AF: 0.453

Gnomad4 FIN AF: 0.471

Gnomad4 NFE AF: 0.414

Gnomad4 OTH AF: 0.407

Alfa AF: 0.410 Hom.: 11932

Bravo AF: 0.380

Asia WGS AF: 0.482 AC: 1674 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
Cadd	Benign	3.1
Dann	Benign	0.76

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: rs3852402; hg19: chr9-98023937;