rs1411766

chr13-109599813-G-Achr13-109599813-G-T

Variant summary

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

The ENST00000650264.1(ENSG00000285534):n.759-28655C>T 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 0.276 in 152,038 control chromosomes in the GnomAD database, including 6,886 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 0.28 (6886 hom., cov: 32)
• Consequence: ENST00000650264.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.181

Genes affected

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.368 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LOC124903210	XR_007063870.1	n.940+6396C>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
	ENST00000650264.1	n.759-28655C>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.276 AC: 41967 AN: 151920 Hom.: 6884 Cov.: 32

Gnomad AFR AF: 0.113

Gnomad AMI AF: 0.465

Gnomad AMR AF: 0.295

Gnomad ASJ AF: 0.321

Gnomad EAS AF: 0.0932

Gnomad SAS AF: 0.153

Gnomad FIN AF: 0.389

Gnomad MID AF: 0.348

Gnomad NFE AF: 0.371

Gnomad OTH AF: 0.283

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

GnomAD4 genome AF: 0.276 AC: 41967 AN: 152038 Hom.: 6886 Cov.: 32 AF XY: 0.273 AC XY: 20271 AN XY: 74304

Gnomad4 AFR AF: 0.112

Gnomad4 AMR AF: 0.295

Gnomad4 ASJ AF: 0.321

Gnomad4 EAS AF: 0.0928

Gnomad4 SAS AF: 0.153

Gnomad4 FIN AF: 0.389

Gnomad4 NFE AF: 0.371

Gnomad4 OTH AF: 0.284

Alfa AF: 0.337 Hom.: 12394

Bravo AF: 0.266

Asia WGS AF: 0.150 AC: 522 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
Cadd	Benign	2.8
Dann	Benign	0.95

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1411766; hg19: chr13-110252160;