chr1-224838965-C-T

Variant names:

• chr1-224838965-C-T
• rs2405783
• ENST00000657178.1:n.78-17977G>A

Variant summary

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

The ENST00000657178.1(ENSG00000286719):​n.78-17977G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.508 in 151,912 control chromosomes in the GnomAD database, including 20,218 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 0.51 (20218 hom., cov: 31)
• Consequence: ENSG00000286719 ENST00000657178.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0810
• Publications: 1 publications found

Genes affected

ENSG00000286719 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.565 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000657178.1. 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
	ENSG00000286719	ENST00000657178.1		n.78-17977G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.508 AC: 77122 AN: 151794 Hom.: 20198 Cov.: 31

Gnomad AFR AF: 0.571

Gnomad AMI AF: 0.479

Gnomad AMR AF: 0.395

Gnomad ASJ AF: 0.531

Gnomad EAS AF: 0.181

Gnomad SAS AF: 0.351

Gnomad FIN AF: 0.540

Gnomad MID AF: 0.611

Gnomad NFE AF: 0.525

Gnomad OTH AF: 0.507

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

GnomAD4 genome AF: 0.508 AC: 77185 AN: 151912 Hom.: 20218 Cov.: 31 AF XY: 0.503 AC XY: 37371 AN XY: 74240

African (AFR) AF: 0.571 AC: 23635 AN: 41400

American (AMR) AF: 0.395 AC: 6031 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.531 AC: 1841 AN: 3470

East Asian (EAS) AF: 0.181 AC: 935 AN: 5162

South Asian (SAS) AF: 0.352 AC: 1693 AN: 4804

European-Finnish (FIN) AF: 0.540 AC: 5690 AN: 10536

Middle Eastern (MID) AF: 0.629 AC: 185 AN: 294

European-Non Finnish (NFE) AF: 0.525 AC: 35667 AN: 67960

Other (OTH) AF: 0.509 AC: 1072 AN: 2108

Alfa AF: 0.513 Hom.: 3641

Bravo AF: 0.498

Asia WGS AF: 0.292 AC: 1015 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	3.2
DANN	Benign	0.51
PhyloP100		0.081

Splicing

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

Other links and lift over

dbSNP: rs2405783; hg19: chr1-225026667;