chr18-60215892-G-A

Variant names:

• chr18-60215892-G-A
• rs646749

Variant summary

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

The variant allele was found at a frequency of 0.453 in 151,886 control chromosomes in the GnomAD database, including 17,316 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 0.45 (17316 hom., cov: 32)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.370
• Publications: 8 publications found

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.671 is higher than 0.05.

Variant Effect in Transcripts

 

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

Frequencies

GnomAD3 genomes AF: 0.453 AC: 68745 AN: 151768 Hom.: 17281 Cov.: 32

Gnomad AFR AF: 0.677

Gnomad AMI AF: 0.404

Gnomad AMR AF: 0.321

Gnomad ASJ AF: 0.296

Gnomad EAS AF: 0.206

Gnomad SAS AF: 0.486

Gnomad FIN AF: 0.346

Gnomad MID AF: 0.439

Gnomad NFE AF: 0.389

Gnomad OTH AF: 0.424

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

GnomAD4 genome AF: 0.453 AC: 68828 AN: 151886 Hom.: 17316 Cov.: 32 AF XY: 0.447 AC XY: 33153 AN XY: 74208

African (AFR) AF: 0.677 AC: 28056 AN: 41424

American (AMR) AF: 0.320 AC: 4883 AN: 15252

Ashkenazi Jewish (ASJ) AF: 0.296 AC: 1025 AN: 3460

East Asian (EAS) AF: 0.206 AC: 1062 AN: 5156

South Asian (SAS) AF: 0.486 AC: 2338 AN: 4812

European-Finnish (FIN) AF: 0.346 AC: 3643 AN: 10536

Middle Eastern (MID) AF: 0.438 AC: 128 AN: 292

European-Non Finnish (NFE) AF: 0.389 AC: 26431 AN: 67934

Other (OTH) AF: 0.424 AC: 894 AN: 2110

Alfa AF: 0.404 Hom.: 23681

Bravo AF: 0.458

Asia WGS AF: 0.333 AC: 1160 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	3.1
DANN	Benign	0.43
PhyloP100		0.37

Splicing

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

Other links and lift over

dbSNP: rs646749; hg19: chr18-57883125;