rs615382

Positions:

• chr12-50019128-C-A
• chr12-50019128-C-G
• chr12-50019128-C-T

Variant summary

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

The NM_001319999.2(RACGAP1):​c.-4-2409G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.723 in 152,078 control chromosomes in the GnomAD database, including 46,452 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 (46452 hom., cov: 31)
• Consequence: RACGAP1 NM_001319999.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.278

Genes affected

RACGAP1 (HGNC:9804): (Rac GTPase activating protein 1) This gene encodes a GTPase-activating protein (GAP) that is a compoment of the centralspindlin complex. This protein binds activated forms of Rho GTPases and stimulates GTP hydrolysis, which results in negative regulation of Rho-mediated signals. This protein plays a regulatory role in cytokinesis, cell growth, and differentiation. Alternatively spliced transcript variants have been found for this gene. There is a pseudogene for this gene on chromosome 12. [provided by RefSeq, Feb 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.92 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RACGAP1	NM_001319999.2	c.-4-2409G>T		intron_variant		ENST00000312377.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RACGAP1	ENST00000312377.10	c.-4-2409G>T		intron_variant		1	NM_001319999.2	P1

Frequencies

GnomAD3 genomes AF: 0.724 AC: 109983 AN: 151960 Hom.: 46453 Cov.: 31

Gnomad AFR AF: 0.255

Gnomad AMI AF: 0.920

Gnomad AMR AF: 0.805

Gnomad ASJ AF: 0.913

Gnomad EAS AF: 0.922

Gnomad SAS AF: 0.696

Gnomad FIN AF: 0.965

Gnomad MID AF: 0.769

Gnomad NFE AF: 0.926

Gnomad OTH AF: 0.769

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

GnomAD4 genome AF: 0.723 AC: 109988 AN: 152078 Hom.: 46452 Cov.: 31 AF XY: 0.729 AC XY: 54196 AN XY: 74360

Gnomad4 AFR AF: 0.254

Gnomad4 AMR AF: 0.804

Gnomad4 ASJ AF: 0.913

Gnomad4 EAS AF: 0.922

Gnomad4 SAS AF: 0.697

Gnomad4 FIN AF: 0.965

Gnomad4 NFE AF: 0.926

Gnomad4 OTH AF: 0.768

Alfa AF: 0.893 Hom.: 96813

Bravo AF: 0.694

Asia WGS AF: 0.757 AC: 2631 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	1.0
DANN	Benign	0.79

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: rs615382; hg19: chr12-50412911;