ENST00000654689.1:n.183-242A>G

Variant names:

• chr6-16940287-T-C
• rs6459492
• ENST00000654689.1:n.183-242A>G

Variant summary

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

The ENST00000654689.1(ENSG00000287347):​n.183-242A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.921 in 151,980 control chromosomes in the GnomAD database, including 64,674 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 0.92 (64674 hom., cov: 28)
• Consequence: ENSG00000287347 ENST00000654689.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.825
• Publications: 7 publications found

Genes affected

ENSG00000287347 (HGNC:):

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 (AFR) allele frequency at 95% confidence interval = 0.973 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000654689.1. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000287347	ENST00000654689.1		n.183-242A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.921 AC: 139907 AN: 151862 Hom.: 64612 Cov.: 28

Gnomad AFR AF: 0.981

Gnomad AMI AF: 0.892

Gnomad AMR AF: 0.942

Gnomad ASJ AF: 0.949

Gnomad EAS AF: 0.815

Gnomad SAS AF: 0.939

Gnomad FIN AF: 0.890

Gnomad MID AF: 0.975

Gnomad NFE AF: 0.891

Gnomad OTH AF: 0.918

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

GnomAD4 genome AF: 0.921 AC: 140028 AN: 151980 Hom.: 64674 Cov.: 28 AF XY: 0.921 AC XY: 68418 AN XY: 74268

African (AFR) AF: 0.981 AC: 40696 AN: 41484

American (AMR) AF: 0.942 AC: 14365 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.949 AC: 3296 AN: 3472

East Asian (EAS) AF: 0.815 AC: 4184 AN: 5134

South Asian (SAS) AF: 0.940 AC: 4514 AN: 4804

European-Finnish (FIN) AF: 0.890 AC: 9387 AN: 10546

Middle Eastern (MID) AF: 0.976 AC: 287 AN: 294

European-Non Finnish (NFE) AF: 0.891 AC: 60549 AN: 67968

Other (OTH) AF: 0.918 AC: 1940 AN: 2114

Alfa AF: 0.907 Hom.: 88873

Bravo AF: 0.927

Asia WGS AF: 0.886 AC: 3080 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.7
DANN	Benign	0.57
PhyloP100		-0.82

Splicing

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

Other links and lift over

dbSNP: rs6459492; hg19: chr6-16940518;