rs885834

Variant names:

• chr10-49607466-G-A
• rs885834

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 0.483 in 152,066 control chromosomes in the GnomAD database, including 20,337 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 0.48 (20337 hom., cov: 33)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.173

ACMG classification

Verdict is Benign. Variant got -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 = 0.623 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt

Frequencies

GnomAD3 genomes AF: 0.483 AC: 73432 AN: 151948 Hom.: 20343 Cov.: 33

Gnomad AFR AF: 0.229

Gnomad AMI AF: 0.609

Gnomad AMR AF: 0.427

Gnomad ASJ AF: 0.545

Gnomad EAS AF: 0.239

Gnomad SAS AF: 0.550

Gnomad FIN AF: 0.675

Gnomad MID AF: 0.611

Gnomad NFE AF: 0.628

Gnomad OTH AF: 0.505

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

GnomAD4 genome AF: 0.483 AC: 73416 AN: 152066 Hom.: 20337 Cov.: 33 AF XY: 0.484 AC XY: 35965 AN XY: 74316

Gnomad4 AFR AF: 0.229

Gnomad4 AMR AF: 0.426

Gnomad4 ASJ AF: 0.545

Gnomad4 EAS AF: 0.240

Gnomad4 SAS AF: 0.549

Gnomad4 FIN AF: 0.675

Gnomad4 NFE AF: 0.628

Gnomad4 OTH AF: 0.501

Alfa AF: 0.521 Hom.: 2139

Bravo AF: 0.444

Asia WGS AF: 0.405 AC: 1410 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	4.5
DANN	Benign	0.60

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs885834; hg19: chr10-50815512;