11-95734098-G-A

Position:

• chr11-95734098-G-A

Variant summary

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

The variant allele was found at a frequency of 0.297 in 152,010 control chromosomes in the GnomAD database, including 8,066 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 (8066 hom., cov: 31)
• Consequence: intergenic_region
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.749

Genes affected

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.402 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
		n.95734098G>A		intergenic_region

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ENSG00000285842	ENST00000648353.1	n.526-10621G>A		intron_variant

Frequencies

GnomAD3 genomes AF: 0.297 AC: 45175 AN: 151890 Hom.: 8062 Cov.: 31

Gnomad AFR AF: 0.111

Gnomad AMI AF: 0.417

Gnomad AMR AF: 0.286

Gnomad ASJ AF: 0.455

Gnomad EAS AF: 0.224

Gnomad SAS AF: 0.142

Gnomad FIN AF: 0.384

Gnomad MID AF: 0.236

Gnomad NFE AF: 0.406

Gnomad OTH AF: 0.338

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

GnomAD4 genome AF: 0.297 AC: 45183 AN: 152010 Hom.: 8066 Cov.: 31 AF XY: 0.292 AC XY: 21693 AN XY: 74276

Gnomad4 AFR AF: 0.111

Gnomad4 AMR AF: 0.285

Gnomad4 ASJ AF: 0.455

Gnomad4 EAS AF: 0.225

Gnomad4 SAS AF: 0.142

Gnomad4 FIN AF: 0.384

Gnomad4 NFE AF: 0.406

Gnomad4 OTH AF: 0.345

Alfa AF: 0.313 Hom.: 1703

Bravo AF: 0.285

Asia WGS AF: 0.201 AC: 699 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	0.64
DANN	Benign	0.69

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs10831417; hg19: chr11-95467262;