rs9958208

Variant names:

• chr18-43011119-G-A
• rs9958208
• NM_002930.4:c.160+22692C>T

Your query was ambiguous. Multiple possible variants found:

• chr18-43011119-G-A
• chr18-43011119-G-C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_002930.4(RIT2):​c.160+22692C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0947 in 151,872 control chromosomes in the GnomAD database, including 784 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 0.095 (784 hom., cov: 33)
• Consequence: RIT2 NM_002930.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.206
• Publications: 6 publications found

Genes affected

RIT2 (HGNC:10017): (Ras like without CAAX 2) RIN belongs to the RAS (HRAS; MIM 190020) superfamily of small GTPases (Shao et al., 1999 [PubMed 10545207]).[supplied by OMIM, Mar 2008]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.113 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RIT2	NM_002930.4	c.160+22692C>T		intron_variant	Intron 2 of 4	ENST00000326695.10	NP_002921.1
RIT2	NM_001272077.2	c.160+22692C>T		intron_variant	Intron 2 of 5		NP_001259006.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RIT2	ENST00000326695.10	c.160+22692C>T		intron_variant	Intron 2 of 4	1	NM_002930.4	ENSP00000321805.4
RIT2	ENST00000589109.5	c.160+22692C>T		intron_variant	Intron 2 of 5	1		ENSP00000467217.1
RIT2	ENST00000590910.1	c.160+22692C>T		intron_variant	Intron 2 of 5	5		ENSP00000466620.1
RIT2	ENST00000650392.1	n.160+22692C>T		intron_variant	Intron 2 of 6			ENSP00000497708.1

Frequencies

GnomAD3 genomes AF: 0.0948 AC: 14381 AN: 151756 Hom.: 786 Cov.: 33

Gnomad AFR AF: 0.0633

Gnomad AMI AF: 0.151

Gnomad AMR AF: 0.0879

Gnomad ASJ AF: 0.128

Gnomad EAS AF: 0.00407

Gnomad SAS AF: 0.0800

Gnomad FIN AF: 0.133

Gnomad MID AF: 0.0791

Gnomad NFE AF: 0.115

Gnomad OTH AF: 0.102

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

GnomAD4 genome AF: 0.0947 AC: 14379 AN: 151872 Hom.: 784 Cov.: 33 AF XY: 0.0946 AC XY: 7017 AN XY: 74210

African (AFR) AF: 0.0633 AC: 2626 AN: 41512

American (AMR) AF: 0.0877 AC: 1333 AN: 15198

Ashkenazi Jewish (ASJ) AF: 0.128 AC: 443 AN: 3460

East Asian (EAS) AF: 0.00408 AC: 21 AN: 5146

South Asian (SAS) AF: 0.0799 AC: 386 AN: 4830

European-Finnish (FIN) AF: 0.133 AC: 1404 AN: 10574

Middle Eastern (MID) AF: 0.0612 AC: 18 AN: 294

European-Non Finnish (NFE) AF: 0.115 AC: 7799 AN: 67840

Other (OTH) AF: 0.100 AC: 211 AN: 2106

Alfa AF: 0.102 Hom.: 1576

Bravo AF: 0.0902

Asia WGS AF: 0.0360 AC: 126 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	3.4
DANN	Benign	0.73
PhyloP100		-0.21
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs9958208; hg19: chr18-40591084;