chr11-95734056-A-G

Variant names:

• chr11-95734056-A-G
• rs10831416
• ENST00000648353.1:n.526-10663A>G

Variant summary

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

The ENST00000648353.1(ENSG00000285842):​n.526-10663A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.297 in 152,008 control chromosomes in the GnomAD database, including 8,056 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 0.30 (8056 hom., cov: 31)
• Consequence: ENSG00000285842 ENST00000648353.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.115
• Publications: 2 publications found

Genes affected

ENSG00000285842 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.402 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000648353.1. 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

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000285842	ENST00000648353.1		n.526-10663A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.297 AC: 45161 AN: 151890 Hom.: 8052 Cov.: 31

Gnomad AFR AF: 0.111

Gnomad AMI AF: 0.415

Gnomad AMR AF: 0.285

Gnomad ASJ AF: 0.455

Gnomad EAS AF: 0.224

Gnomad SAS AF: 0.142

Gnomad FIN AF: 0.384

Gnomad MID AF: 0.237

Gnomad NFE AF: 0.406

Gnomad OTH AF: 0.337

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

GnomAD4 genome AF: 0.297 AC: 45168 AN: 152008 Hom.: 8056 Cov.: 31 AF XY: 0.292 AC XY: 21692 AN XY: 74290

African (AFR) AF: 0.110 AC: 4583 AN: 41478

American (AMR) AF: 0.285 AC: 4344 AN: 15266

Ashkenazi Jewish (ASJ) AF: 0.455 AC: 1576 AN: 3464

East Asian (EAS) AF: 0.225 AC: 1162 AN: 5174

South Asian (SAS) AF: 0.142 AC: 685 AN: 4820

European-Finnish (FIN) AF: 0.384 AC: 4048 AN: 10544

Middle Eastern (MID) AF: 0.241 AC: 71 AN: 294

European-Non Finnish (NFE) AF: 0.406 AC: 27598 AN: 67954

Other (OTH) AF: 0.344 AC: 725 AN: 2108

Alfa AF: 0.336 Hom.: 1279

Bravo AF: 0.285

Asia WGS AF: 0.201 AC: 699 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	4.8
DANN	Benign	0.69
PhyloP100		0.12

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs10831416; hg19: chr11-95467220;