rs2769605

Positions:

• chr9-85297756-C-T

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 0.439 in 152,102 control chromosomes in the GnomAD database, including 16,667 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 0.44 (16667 hom., cov: 33)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.203

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.561 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: 0.439 AC: 66748 AN: 151984 Hom.: 16674 Cov.: 33

Gnomad AFR AF: 0.214

Gnomad AMI AF: 0.537

Gnomad AMR AF: 0.423

Gnomad ASJ AF: 0.537

Gnomad EAS AF: 0.194

Gnomad SAS AF: 0.579

Gnomad FIN AF: 0.538

Gnomad MID AF: 0.636

Gnomad NFE AF: 0.565

Gnomad OTH AF: 0.476

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

GnomAD4 genome AF: 0.439 AC: 66751 AN: 152102 Hom.: 16667 Cov.: 33 AF XY: 0.439 AC XY: 32633 AN XY: 74352

Gnomad4 AFR AF: 0.214

Gnomad4 AMR AF: 0.423

Gnomad4 ASJ AF: 0.537

Gnomad4 EAS AF: 0.194

Gnomad4 SAS AF: 0.579

Gnomad4 FIN AF: 0.538

Gnomad4 NFE AF: 0.565

Gnomad4 OTH AF: 0.474

Alfa AF: 0.498 Hom.: 5029

Bravo AF: 0.412

Asia WGS AF: 0.376 AC: 1310 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	1.3
DANN	Benign	0.53

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs2769605; hg19: chr9-87912671;