rs1060402

chr20-50588558-G-A

Variant summary

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

The NM_001290268.2(RIPOR3):c.2662-666C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.459 in 151,858 control chromosomes in the GnomAD database, including 16,813 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 0.46 (16813 hom., cov: 32)
• Consequence: RIPOR3 NM_001290268.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.104

Genes affected

RIPOR3 (HGNC:16168): (RIPOR family member 3)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.605 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RIPOR3	NM_001290268.2	c.2662-666C>T		intron_variant		ENST00000327979.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RIPOR3	ENST00000327979.8	c.2662-666C>T		intron_variant		2	NM_001290268.2
RIPOR3	ENST00000045083.6	c.2650-666C>T		intron_variant		5		P1
RIPOR3	ENST00000462842.1	n.328-666C>T		intron_variant, non_coding_transcript_variant		2

Frequencies

GnomAD3 genomes AF: 0.459 AC: 69697 AN: 151744 Hom.: 16814 Cov.: 32

Gnomad AFR AF: 0.299

Gnomad AMI AF: 0.577

Gnomad AMR AF: 0.473

Gnomad ASJ AF: 0.534

Gnomad EAS AF: 0.623

Gnomad SAS AF: 0.607

Gnomad FIN AF: 0.540

Gnomad MID AF: 0.623

Gnomad NFE AF: 0.512

Gnomad OTH AF: 0.483

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

GnomAD4 genome AF: 0.459 AC: 69712 AN: 151858 Hom.: 16813 Cov.: 32 AF XY: 0.462 AC XY: 34283 AN XY: 74208

Gnomad4 AFR AF: 0.298

Gnomad4 AMR AF: 0.473

Gnomad4 ASJ AF: 0.534

Gnomad4 EAS AF: 0.623

Gnomad4 SAS AF: 0.607

Gnomad4 FIN AF: 0.540

Gnomad4 NFE AF: 0.512

Gnomad4 OTH AF: 0.485

Alfa AF: 0.497 Hom.: 9038

Bravo AF: 0.447

Asia WGS AF: 0.583 AC: 2027 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
Cadd	Benign	1.4
Dann	Benign	0.51

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: rs1060402; hg19: chr20-49205095;