ENST00000651871.1:n.789-3381A>G

Variant names:

• chr20-48331510-T-C
• rs6019048
• ENST00000651871.1:n.789-3381A>G

Variant summary

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

The ENST00000651871.1(ENSG00000286063):​n.789-3381A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0362 in 152,336 control chromosomes in the GnomAD database, including 196 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 0.036 (196 hom., cov: 32)
• Consequence: ENSG00000286063 ENST00000651871.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0790
• Publications: 1 publications found

Genes affected

ENSG00000286063 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.122 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000651871.1. You can select a different transcript below to see updated ACMG assignments.

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
	ENSG00000286063	ENST00000651871.1		n.789-3381A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.0360 AC: 5484 AN: 152218 Hom.: 193 Cov.: 32

Gnomad AFR AF: 0.0729

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0501

Gnomad ASJ AF: 0.00346

Gnomad EAS AF: 0.130

Gnomad SAS AF: 0.0246

Gnomad FIN AF: 0.0208

Gnomad MID AF: 0.0158

Gnomad NFE AF: 0.00875

Gnomad OTH AF: 0.0339

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

GnomAD4 genome AF: 0.0362 AC: 5515 AN: 152336 Hom.: 196 Cov.: 32 AF XY: 0.0371 AC XY: 2764 AN XY: 74496

African (AFR) AF: 0.0733 AC: 3048 AN: 41576

American (AMR) AF: 0.0503 AC: 770 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.00346 AC: 12 AN: 3470

East Asian (EAS) AF: 0.130 AC: 674 AN: 5184

South Asian (SAS) AF: 0.0246 AC: 119 AN: 4834

European-Finnish (FIN) AF: 0.0208 AC: 221 AN: 10624

Middle Eastern (MID) AF: 0.0170 AC: 5 AN: 294

European-Non Finnish (NFE) AF: 0.00873 AC: 594 AN: 68030

Other (OTH) AF: 0.0340 AC: 72 AN: 2116

Alfa AF: 0.0176 Hom.: 212

Bravo AF: 0.0405

Asia WGS AF: 0.0940 AC: 326 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.8
DANN	Benign	0.78
PhyloP100		-0.079

Splicing

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

Other links and lift over

dbSNP: rs6019048; hg19: chr20-46960253;