chr6-24898851-A-G

Position:

• chr6-24898851-A-G

Variant summary

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

The NM_001286445.3(RIPOR2):​c.62-23034T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.731 in 152,002 control chromosomes in the GnomAD database, including 41,861 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 0.73 (41861 hom., cov: 31)
• Consequence: RIPOR2 NM_001286445.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.715

Genes affected

RIPOR2 (HGNC:13872): (RHO family interacting cell polarization regulator 2) This gene encodes an atypical inhibitor of the small G protein RhoA. Inhibition of RhoA activity by the encoded protein mediates myoblast fusion and polarization of T cells and neutrophils. The encoded protein is a component of hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients. [provided by RefSeq, Sep 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.922 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RIPOR2	NM_001286445.3	c.62-23034T>C		intron_variant		ENST00000643898.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RIPOR2	ENST00000643898.2	c.62-23034T>C		intron_variant			NM_001286445.3	A2

Frequencies

GnomAD3 genomes AF: 0.731 AC: 111000 AN: 151884 Hom.: 41784 Cov.: 31

Gnomad AFR AF: 0.930

Gnomad AMI AF: 0.595

Gnomad AMR AF: 0.720

Gnomad ASJ AF: 0.586

Gnomad EAS AF: 0.609

Gnomad SAS AF: 0.704

Gnomad FIN AF: 0.687

Gnomad MID AF: 0.669

Gnomad NFE AF: 0.640

Gnomad OTH AF: 0.715

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

GnomAD4 genome AF: 0.731 AC: 111138 AN: 152002 Hom.: 41861 Cov.: 31 AF XY: 0.731 AC XY: 54317 AN XY: 74272

Gnomad4 AFR AF: 0.930

Gnomad4 AMR AF: 0.720

Gnomad4 ASJ AF: 0.586

Gnomad4 EAS AF: 0.609

Gnomad4 SAS AF: 0.704

Gnomad4 FIN AF: 0.687

Gnomad4 NFE AF: 0.640

Gnomad4 OTH AF: 0.718

Alfa AF: 0.641 Hom.: 12434

Bravo AF: 0.737

Asia WGS AF: 0.685 AC: 2382 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.2
DANN	Benign	0.78

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: rs926850; hg19: chr6-24899079;