chr3-109132944-A-G

Variant names:

• chr3-109132944-A-G
• rs4441659
• ENST00000479039.3:n.145-3900A>G

Variant summary

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

The ENST00000479039.3(C3orf85):​n.145-3900A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.798 in 152,078 control chromosomes in the GnomAD database, including 49,185 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 0.80 (49185 hom., cov: 31)
• Consequence: C3orf85 ENST00000479039.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.09
• Publications: 7 publications found

Genes affected

C3orf85 (HGNC:53432): (chromosome 3 open reading frame 85)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.904 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000479039.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	C3orf85	ENST00000479039.3	TSL:5	n.145-3900A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.798 AC: 121270 AN: 151960 Hom.: 49148 Cov.: 31

Gnomad AFR AF: 0.649

Gnomad AMI AF: 0.880

Gnomad AMR AF: 0.863

Gnomad ASJ AF: 0.794

Gnomad EAS AF: 0.926

Gnomad SAS AF: 0.848

Gnomad FIN AF: 0.889

Gnomad MID AF: 0.750

Gnomad NFE AF: 0.846

Gnomad OTH AF: 0.800

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

GnomAD4 genome AF: 0.798 AC: 121356 AN: 152078 Hom.: 49185 Cov.: 31 AF XY: 0.802 AC XY: 59665 AN XY: 74360

African (AFR) AF: 0.649 AC: 26896 AN: 41444

American (AMR) AF: 0.863 AC: 13190 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.794 AC: 2756 AN: 3470

East Asian (EAS) AF: 0.926 AC: 4788 AN: 5172

South Asian (SAS) AF: 0.847 AC: 4079 AN: 4814

European-Finnish (FIN) AF: 0.889 AC: 9406 AN: 10586

Middle Eastern (MID) AF: 0.772 AC: 227 AN: 294

European-Non Finnish (NFE) AF: 0.846 AC: 57534 AN: 67994

Other (OTH) AF: 0.795 AC: 1679 AN: 2112

Alfa AF: 0.832 Hom.: 213988

Bravo AF: 0.790

Asia WGS AF: 0.857 AC: 2981 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	0.29
DANN	Benign	0.33
PhyloP100		-2.1

Splicing

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

Other links and lift over

dbSNP: rs4441659; hg19: chr3-108851791;