rs4922116

Variant names:

• chr8-19975267-G-A
• rs4922116

Your query was ambiguous. Multiple possible variants found:

• chr8-19975267-G-A
• chr8-19975267-G-T

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 0.161 in 152,062 control chromosomes in the GnomAD database, including 2,037 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 0.16 (2037 hom., cov: 32)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.14
• Publications: 6 publications found

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.164 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: 0.161 AC: 24480 AN: 151944 Hom.: 2034 Cov.: 32

Gnomad AFR AF: 0.154

Gnomad AMI AF: 0.239

Gnomad AMR AF: 0.162

Gnomad ASJ AF: 0.236

Gnomad EAS AF: 0.0981

Gnomad SAS AF: 0.155

Gnomad FIN AF: 0.158

Gnomad MID AF: 0.174

Gnomad NFE AF: 0.166

Gnomad OTH AF: 0.159

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

GnomAD4 genome AF: 0.161 AC: 24506 AN: 152062 Hom.: 2037 Cov.: 32 AF XY: 0.160 AC XY: 11922 AN XY: 74346

African (AFR) AF: 0.154 AC: 6377 AN: 41466

American (AMR) AF: 0.162 AC: 2476 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.236 AC: 821 AN: 3472

East Asian (EAS) AF: 0.0983 AC: 508 AN: 5168

South Asian (SAS) AF: 0.156 AC: 750 AN: 4818

European-Finnish (FIN) AF: 0.158 AC: 1672 AN: 10564

Middle Eastern (MID) AF: 0.180 AC: 53 AN: 294

European-Non Finnish (NFE) AF: 0.166 AC: 11292 AN: 67988

Other (OTH) AF: 0.161 AC: 339 AN: 2112

Alfa AF: 0.163 Hom.: 432

Bravo AF: 0.159

Asia WGS AF: 0.145 AC: 503 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.018
DANN	Benign	0.29
PhyloP100		-2.1

Splicing

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

Other links and lift over

dbSNP: rs4922116; hg19: chr8-19832778;