ENST00000587346.1:n.140-4288C>T

Variant names:

• chr18-55757015-C-T
• rs784233
• ENST00000587346.1:n.140-4288C>T

Variant summary

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

The ENST00000587346.1(ENSG00000267284):​n.140-4288C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.083 in 152,050 control chromosomes in the GnomAD database, including 908 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 0.083 (908 hom., cov: 29)
• Consequence: ENSG00000267284 ENST00000587346.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.157
• Publications: 2 publications found

Genes affected

ENSG00000267284 (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 (EAS) allele frequency at 95% confidence interval = 0.345 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LOC105372130	XR_007066382.1	n.329-27884C>T		intron_variant	Intron 2 of 8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ENSG00000267284	ENST00000587346.1	n.140-4288C>T		intron_variant	Intron 1 of 4	4
ENSG00000267284	ENST00000589662.1	n.218-27884C>T		intron_variant	Intron 1 of 3	5
ENSG00000267284	ENST00000592936.1	n.473-2025C>T		intron_variant	Intron 1 of 1	4

Frequencies

GnomAD3 genomes AF: 0.0829 AC: 12593 AN: 151932 Hom.: 909 Cov.: 29

Gnomad AFR AF: 0.139

Gnomad AMI AF: 0.0340

Gnomad AMR AF: 0.0350

Gnomad ASJ AF: 0.0236

Gnomad EAS AF: 0.358

Gnomad SAS AF: 0.175

Gnomad FIN AF: 0.0528

Gnomad MID AF: 0.0222

Gnomad NFE AF: 0.0412

Gnomad OTH AF: 0.0662

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

GnomAD4 genome AF: 0.0830 AC: 12613 AN: 152050 Hom.: 908 Cov.: 29 AF XY: 0.0845 AC XY: 6282 AN XY: 74314

African (AFR) AF: 0.139 AC: 5776 AN: 41448

American (AMR) AF: 0.0350 AC: 534 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.0236 AC: 82 AN: 3468

East Asian (EAS) AF: 0.359 AC: 1842 AN: 5136

South Asian (SAS) AF: 0.175 AC: 843 AN: 4814

European-Finnish (FIN) AF: 0.0528 AC: 559 AN: 10588

Middle Eastern (MID) AF: 0.0204 AC: 6 AN: 294

European-Non Finnish (NFE) AF: 0.0412 AC: 2800 AN: 68006

Other (OTH) AF: 0.0664 AC: 140 AN: 2108

Alfa AF: 0.0500 Hom.: 284

Bravo AF: 0.0830

Asia WGS AF: 0.226 AC: 786 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	1.8
DANN	Benign	0.43
PhyloP100		-0.16

Splicing

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

Other links and lift over

dbSNP: rs784233; hg19: chr18-53424246;