rs2924567

chr15-47976289-G-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000657831.1(ENSG00000287439):n.408+11348C>A variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.251 in 152,038 control chromosomes in the GnomAD database, including 6,209 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 0.25 (6209 hom., cov: 31)
• Consequence: ENST00000657831.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.674

Genes affected

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.357 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LOC124900354	XR_001751516.3	n.143-16420G>T		intron_variant, non_coding_transcript_variant
LOC102724553	XR_001751520.2	n.480+11348C>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
	ENST00000657831.1	n.408+11348C>A		intron_variant, non_coding_transcript_variant
	ENST00000662551.1	n.189-16420G>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.251 AC: 38207 AN: 151920 Hom.: 6216 Cov.: 31

Gnomad AFR AF: 0.0693

Gnomad AMI AF: 0.361

Gnomad AMR AF: 0.274

Gnomad ASJ AF: 0.388

Gnomad EAS AF: 0.00270

Gnomad SAS AF: 0.257

Gnomad FIN AF: 0.279

Gnomad MID AF: 0.465

Gnomad NFE AF: 0.361

Gnomad OTH AF: 0.295

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

GnomAD4 genome AF: 0.251 AC: 38188 AN: 152038 Hom.: 6209 Cov.: 31 AF XY: 0.248 AC XY: 18422 AN XY: 74306

Gnomad4 AFR AF: 0.0691

Gnomad4 AMR AF: 0.273

Gnomad4 ASJ AF: 0.388

Gnomad4 EAS AF: 0.00271

Gnomad4 SAS AF: 0.258

Gnomad4 FIN AF: 0.279

Gnomad4 NFE AF: 0.361

Gnomad4 OTH AF: 0.291

Alfa AF: 0.282 Hom.: 1184

Bravo AF: 0.242

Asia WGS AF: 0.108 AC: 374 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
Cadd	Benign	0.43
Dann	Benign	0.35

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs2924567; hg19: chr15-48268486;