rs6790891

chr3-71910159-T-C

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 0.129 in 152,202 control chromosomes in the GnomAD database, including 1,298 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 (1298 hom., cov: 32)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.893

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.132 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt

Frequencies

GnomAD3 genomes AF: 0.129 AC: 19587 AN: 152084 Hom.: 1299 Cov.: 32

Gnomad AFR AF: 0.134

Gnomad AMI AF: 0.172

Gnomad AMR AF: 0.0952

Gnomad ASJ AF: 0.106

Gnomad EAS AF: 0.128

Gnomad SAS AF: 0.0949

Gnomad FIN AF: 0.138

Gnomad MID AF: 0.146

Gnomad NFE AF: 0.135

Gnomad OTH AF: 0.126

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

GnomAD4 genome AF: 0.129 AC: 19588 AN: 152202 Hom.: 1298 Cov.: 32 AF XY: 0.126 AC XY: 9386 AN XY: 74400

Gnomad4 AFR AF: 0.134

Gnomad4 AMR AF: 0.0950

Gnomad4 ASJ AF: 0.106

Gnomad4 EAS AF: 0.128

Gnomad4 SAS AF: 0.0936

Gnomad4 FIN AF: 0.138

Gnomad4 NFE AF: 0.135

Gnomad4 OTH AF: 0.128

Alfa AF: 0.129 Hom.: 1374

Bravo AF: 0.124

Asia WGS AF: 0.124 AC: 433 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
Cadd	Benign	2.6
Dann	Benign	0.41

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs6790891; hg19: chr3-71959310;