rs11214105

chr11-112166930-G-A

Variant summary

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

The ENST00000527589.1(ENSG00000254638):n.171-754C>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 0.251 in 152,026 control chromosomes in the GnomAD database, including 4,996 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 (4996 hom., cov: 32)
• Consequence: ENST00000527589.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.794

Genes affected

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.29 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LOC107987164	XR_001748384.2	n.81+133C>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
	ENST00000527589.1	n.171-754C>T		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.251 AC: 38170 AN: 151908 Hom.: 4997 Cov.: 32

Gnomad AFR AF: 0.210

Gnomad AMI AF: 0.236

Gnomad AMR AF: 0.297

Gnomad ASJ AF: 0.268

Gnomad EAS AF: 0.128

Gnomad SAS AF: 0.214

Gnomad FIN AF: 0.287

Gnomad MID AF: 0.268

Gnomad NFE AF: 0.272

Gnomad OTH AF: 0.249

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

GnomAD4 genome AF: 0.251 AC: 38161 AN: 152026 Hom.: 4996 Cov.: 32 AF XY: 0.251 AC XY: 18645 AN XY: 74290

Gnomad4 AFR AF: 0.209

Gnomad4 AMR AF: 0.297

Gnomad4 ASJ AF: 0.268

Gnomad4 EAS AF: 0.127

Gnomad4 SAS AF: 0.213

Gnomad4 FIN AF: 0.287

Gnomad4 NFE AF: 0.272

Gnomad4 OTH AF: 0.246

Alfa AF: 0.267 Hom.: 5395

Bravo AF: 0.252

Asia WGS AF: 0.185 AC: 646 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
Cadd	Benign	0.85
Dann	Benign	0.60

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Publications

LitVar

Other links and lift over

dbSNP: rs11214105; hg19: chr11-112037653;