chr13-33093328-G-A

Variant names:

• chr13-33093328-G-A
• rs648464

Variant summary

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

The variant allele was found at a frequency of 0.364 in 151,802 control chromosomes in the GnomAD database, including 10,252 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 0.36 (10252 hom., cov: 31)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.614
• Publications: 2 publications found

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 (EAS) allele frequency at 95% confidence interval = 0.441 is higher than 0.05.

Variant Effect in Transcripts

 

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

Frequencies

GnomAD3 genomes AF: 0.364 AC: 55258 AN: 151684 Hom.: 10253 Cov.: 31

Gnomad AFR AF: 0.345

Gnomad AMI AF: 0.491

Gnomad AMR AF: 0.313

Gnomad ASJ AF: 0.404

Gnomad EAS AF: 0.456

Gnomad SAS AF: 0.436

Gnomad FIN AF: 0.418

Gnomad MID AF: 0.405

Gnomad NFE AF: 0.364

Gnomad OTH AF: 0.362

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

GnomAD4 genome AF: 0.364 AC: 55258 AN: 151802 Hom.: 10252 Cov.: 31 AF XY: 0.367 AC XY: 27213 AN XY: 74148

African (AFR) AF: 0.344 AC: 14248 AN: 41392

American (AMR) AF: 0.312 AC: 4760 AN: 15266

Ashkenazi Jewish (ASJ) AF: 0.404 AC: 1402 AN: 3468

East Asian (EAS) AF: 0.456 AC: 2347 AN: 5144

South Asian (SAS) AF: 0.436 AC: 2077 AN: 4760

European-Finnish (FIN) AF: 0.418 AC: 4412 AN: 10556

Middle Eastern (MID) AF: 0.398 AC: 117 AN: 294

European-Non Finnish (NFE) AF: 0.364 AC: 24696 AN: 67908

Other (OTH) AF: 0.357 AC: 751 AN: 2102

Alfa AF: 0.360 Hom.: 10260

Bravo AF: 0.353

Asia WGS AF: 0.406 AC: 1407 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.21
DANN	Benign	0.55
PhyloP100		-0.61

Splicing

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

Other links and lift over

dbSNP: rs648464; hg19: chr13-33667465; COSMIC: COSV69346349;