15-96367211-T-C

Position:

• chr15-96367211-T-C

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The ENST00000664133.1(ENSG00000259275):​n.166+12699T>C 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 0.502 in 152,162 control chromosomes in the GnomAD database, including 19,583 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 0.50 (19583 hom., cov: 34)
• Consequence: ENST00000664133.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.28

Genes affected

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.38).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.564 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
LOC101927263	XR_007064788.1	n.1281-5198T>C		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
	ENST00000664133.1	n.166+12699T>C		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.502 AC: 76278 AN: 152046 Hom.: 19575 Cov.: 34

Gnomad AFR AF: 0.404

Gnomad AMI AF: 0.617

Gnomad AMR AF: 0.486

Gnomad ASJ AF: 0.543

Gnomad EAS AF: 0.308

Gnomad SAS AF: 0.431

Gnomad FIN AF: 0.577

Gnomad MID AF: 0.538

Gnomad NFE AF: 0.569

Gnomad OTH AF: 0.492

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

GnomAD4 genome AF: 0.502 AC: 76319 AN: 152162 Hom.: 19583 Cov.: 34 AF XY: 0.498 AC XY: 37058 AN XY: 74368

Gnomad4 AFR AF: 0.404

Gnomad4 AMR AF: 0.486

Gnomad4 ASJ AF: 0.543

Gnomad4 EAS AF: 0.307

Gnomad4 SAS AF: 0.431

Gnomad4 FIN AF: 0.577

Gnomad4 NFE AF: 0.569

Gnomad4 OTH AF: 0.496

Alfa AF: 0.551 Hom.: 49253

Bravo AF: 0.491

Asia WGS AF: 0.413 AC: 1429 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.38
CADD	Benign	15
DANN	Benign	0.79

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs8031676; hg19: chr15-96910440;