rs4738902

Variant names:

• chr8-61495359-C-A
• rs4738902
• NM_173519.3:c.978-4096C>A

Your query was ambiguous. Multiple possible variants found:

• chr8-61495359-C-A
• chr8-61495359-C-G

Variant summary

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

The NM_173519.3(CLVS1):​c.978-4096C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.559 in 152,044 control chromosomes in the GnomAD database, including 26,834 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 0.56 (26834 hom., cov: 32)
• Consequence: CLVS1 NM_173519.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.293
• Publications: 2 publications found

Genes affected

CLVS1 (HGNC:23139): (clavesin 1) Enables phosphatidylinositol-3,5-bisphosphate binding activity. Predicted to be involved in lysosome organization. Located in endosome. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.703 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CLVS1	NM_173519.3	c.978-4096C>A		intron_variant	Intron 5 of 5	ENST00000325897.5	NP_775790.1
CLVS1	XM_017013141.2	c.978-4096C>A		intron_variant	Intron 6 of 6		XP_016868630.1
CLVS1	XM_017013142.3	c.978-4096C>A		intron_variant	Intron 6 of 6		XP_016868631.1
CLVS1	XM_024447079.2	c.978-4096C>A		intron_variant	Intron 8 of 8		XP_024302847.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CLVS1	ENST00000325897.5	c.978-4096C>A		intron_variant	Intron 5 of 5	1	NM_173519.3	ENSP00000325506.4

Frequencies

GnomAD3 genomes AF: 0.559 AC: 84915 AN: 151928 Hom.: 26814 Cov.: 32

Gnomad AFR AF: 0.248

Gnomad AMI AF: 0.760

Gnomad AMR AF: 0.597

Gnomad ASJ AF: 0.615

Gnomad EAS AF: 0.478

Gnomad SAS AF: 0.639

Gnomad FIN AF: 0.720

Gnomad MID AF: 0.652

Gnomad NFE AF: 0.709

Gnomad OTH AF: 0.573

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

GnomAD4 genome AF: 0.559 AC: 84956 AN: 152044 Hom.: 26834 Cov.: 32 AF XY: 0.559 AC XY: 41535 AN XY: 74318

African (AFR) AF: 0.248 AC: 10296 AN: 41490

American (AMR) AF: 0.597 AC: 9110 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.615 AC: 2137 AN: 3472

East Asian (EAS) AF: 0.478 AC: 2464 AN: 5158

South Asian (SAS) AF: 0.642 AC: 3095 AN: 4820

European-Finnish (FIN) AF: 0.720 AC: 7597 AN: 10556

Middle Eastern (MID) AF: 0.646 AC: 190 AN: 294

European-Non Finnish (NFE) AF: 0.709 AC: 48161 AN: 67976

Other (OTH) AF: 0.575 AC: 1213 AN: 2110

Alfa AF: 0.642 Hom.: 16848

Bravo AF: 0.536

Asia WGS AF: 0.570 AC: 1985 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	1.0
DANN	Benign	0.42
PhyloP100		-0.29
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: rs4738902; hg19: chr8-62407918;