chr8-109062879-T-C

Variant names:

• chr8-109062879-T-C
• rs4469428
• ENST00000522244.1:n.129+410A>G

Variant summary

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

The ENST00000522244.1(ENSG00000253796):​n.129+410A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.672 in 152,108 control chromosomes in the GnomAD database, including 35,076 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 0.67 (35076 hom., cov: 32)
• Consequence: ENSG00000253796 ENST00000522244.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0880
• Publications: 0 publications found

Genes affected

ENSG00000253796 (HGNC:):

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 (AFR) allele frequency at 95% confidence interval = 0.789 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000522244.1. 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
	ENSG00000253796	ENST00000522244.1	TSL:3	n.129+410A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.671 AC: 102038 AN: 151990 Hom.: 35033 Cov.: 32

Gnomad AFR AF: 0.796

Gnomad AMI AF: 0.732

Gnomad AMR AF: 0.749

Gnomad ASJ AF: 0.544

Gnomad EAS AF: 0.717

Gnomad SAS AF: 0.714

Gnomad FIN AF: 0.590

Gnomad MID AF: 0.516

Gnomad NFE AF: 0.591

Gnomad OTH AF: 0.659

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

GnomAD4 genome AF: 0.672 AC: 102143 AN: 152108 Hom.: 35076 Cov.: 32 AF XY: 0.675 AC XY: 50205 AN XY: 74350

African (AFR) AF: 0.796 AC: 33046 AN: 41512

American (AMR) AF: 0.749 AC: 11453 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.544 AC: 1886 AN: 3470

East Asian (EAS) AF: 0.718 AC: 3713 AN: 5168

South Asian (SAS) AF: 0.714 AC: 3443 AN: 4820

European-Finnish (FIN) AF: 0.590 AC: 6237 AN: 10566

Middle Eastern (MID) AF: 0.514 AC: 151 AN: 294

European-Non Finnish (NFE) AF: 0.591 AC: 40150 AN: 67962

Other (OTH) AF: 0.660 AC: 1396 AN: 2116

Alfa AF: 0.647 Hom.: 5636

Bravo AF: 0.689

Asia WGS AF: 0.736 AC: 2559 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	6.4
DANN	Benign	0.50
PhyloP100		-0.088

Splicing

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

Other links and lift over

dbSNP: rs4469428; hg19: chr8-110075108;