rs10517263

Variant names:

• chr4-52632502-G-C
• rs10517263
• NM_022832.4:c.37-1358C>G

Variant summary

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

The NM_022832.4(USP46):​c.37-1358C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.135 in 152,070 control chromosomes in the GnomAD database, including 1,437 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 0.13 (1437 hom., cov: 31)
• Consequence: USP46 NM_022832.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.794
• Publications: 6 publications found

Genes affected

USP46 (HGNC:20075): (ubiquitin specific peptidase 46) Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP46 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Jun 2009]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.187 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_022832.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	USP46	NM_022832.4	MANE Select	c.37-1358C>G		intron	N/A	NP_073743.2
	USP46	NM_001134223.2		c.16-1358C>G		intron	N/A	NP_001127695.1
	USP46	NM_001286767.2		c.37-1358C>G		intron	N/A	NP_001273696.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	USP46	ENST00000441222.8	TSL:1 MANE Select	c.37-1358C>G		intron	N/A	ENSP00000407818.2
	USP46	ENST00000508499.5	TSL:2	c.16-1358C>G		intron	N/A	ENSP00000423244.1
	USP46	ENST00000451218.6	TSL:5	c.37-4339C>G		intron	N/A	ENSP00000390102.2

Frequencies

GnomAD3 genomes AF: 0.134 AC: 20427 AN: 151952 Hom.: 1426 Cov.: 31

Gnomad AFR AF: 0.190

Gnomad AMI AF: 0.106

Gnomad AMR AF: 0.122

Gnomad ASJ AF: 0.102

Gnomad EAS AF: 0.109

Gnomad SAS AF: 0.0944

Gnomad FIN AF: 0.116

Gnomad MID AF: 0.0981

Gnomad NFE AF: 0.113

Gnomad OTH AF: 0.139

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

GnomAD4 genome AF: 0.135 AC: 20483 AN: 152070 Hom.: 1437 Cov.: 31 AF XY: 0.135 AC XY: 10024 AN XY: 74340

African (AFR) AF: 0.191 AC: 7901 AN: 41440

American (AMR) AF: 0.121 AC: 1857 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.102 AC: 353 AN: 3466

East Asian (EAS) AF: 0.108 AC: 555 AN: 5158

South Asian (SAS) AF: 0.0949 AC: 458 AN: 4826

European-Finnish (FIN) AF: 0.116 AC: 1228 AN: 10578

Middle Eastern (MID) AF: 0.105 AC: 31 AN: 294

European-Non Finnish (NFE) AF: 0.113 AC: 7706 AN: 68006

Other (OTH) AF: 0.141 AC: 297 AN: 2106

Alfa AF: 0.125 Hom.: 181

Bravo AF: 0.140

Asia WGS AF: 0.126 AC: 439 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	5.4
DANN	Benign	0.55
PhyloP100		0.79
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: rs10517263; hg19: chr4-53498669;