18-68315119-A-G

Variant names:

• chr18-68315119-A-G
• rs12458992
• ENST00000661028.2:n.644+12844T>C

Variant summary

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

The ENST00000661028.2(ENSG00000287907):​n.644+12844T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.292 in 151,156 control chromosomes in the GnomAD database, including 6,986 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 0.29 (6986 hom., cov: 29)
• Consequence: ENSG00000287907 ENST00000661028.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0720
• Publications: 1 publications found

Genes affected

ENSG00000287907 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.422 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000661028.2. 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
	ENSG00000287907	ENST00000661028.2		n.644+12844T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.292 AC: 44115 AN: 151036 Hom.: 6981 Cov.: 29

Gnomad AFR AF: 0.176

Gnomad AMI AF: 0.348

Gnomad AMR AF: 0.314

Gnomad ASJ AF: 0.378

Gnomad EAS AF: 0.223

Gnomad SAS AF: 0.438

Gnomad FIN AF: 0.301

Gnomad MID AF: 0.301

Gnomad NFE AF: 0.345

Gnomad OTH AF: 0.319

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

GnomAD4 genome AF: 0.292 AC: 44123 AN: 151156 Hom.: 6986 Cov.: 29 AF XY: 0.292 AC XY: 21564 AN XY: 73808

African (AFR) AF: 0.175 AC: 7215 AN: 41124

American (AMR) AF: 0.314 AC: 4767 AN: 15162

Ashkenazi Jewish (ASJ) AF: 0.378 AC: 1307 AN: 3462

East Asian (EAS) AF: 0.222 AC: 1132 AN: 5090

South Asian (SAS) AF: 0.438 AC: 2092 AN: 4776

European-Finnish (FIN) AF: 0.301 AC: 3139 AN: 10424

Middle Eastern (MID) AF: 0.303 AC: 89 AN: 294

European-Non Finnish (NFE) AF: 0.345 AC: 23390 AN: 67818

Other (OTH) AF: 0.322 AC: 675 AN: 2096

Alfa AF: 0.196 Hom.: 452

Bravo AF: 0.284

Asia WGS AF: 0.325 AC: 1131 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	6.7
DANN	Benign	0.56
PhyloP100		0.072

Splicing

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

Other links and lift over

dbSNP: rs12458992; hg19: chr18-65982356;