11-6183086-C-A

Variant names:

• chr11-6183086-C-A
• rs325648
• ENST00000529961.1:n.286+2205G>T

Variant summary

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

The ENST00000529961.1(ENSG00000254444):​n.286+2205G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.657 in 151,988 control chromosomes in the GnomAD database, including 33,978 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 0.66 (33978 hom., cov: 32)
• Consequence: ENSG00000254444 ENST00000529961.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.38
• Publications: 2 publications found

Genes affected

ENSG00000254444 (HGNC:):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.07).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.747 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000529961.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000254444	ENST00000529961.1	TSL:5	n.286+2205G>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.657 AC: 99829 AN: 151870 Hom.: 33961 Cov.: 32

Gnomad AFR AF: 0.478

Gnomad AMI AF: 0.753

Gnomad AMR AF: 0.669

Gnomad ASJ AF: 0.765

Gnomad EAS AF: 0.606

Gnomad SAS AF: 0.527

Gnomad FIN AF: 0.767

Gnomad MID AF: 0.759

Gnomad NFE AF: 0.752

Gnomad OTH AF: 0.673

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

GnomAD4 genome AF: 0.657 AC: 99887 AN: 151988 Hom.: 33978 Cov.: 32 AF XY: 0.655 AC XY: 48670 AN XY: 74272

African (AFR) AF: 0.478 AC: 19787 AN: 41404

American (AMR) AF: 0.669 AC: 10204 AN: 15264

Ashkenazi Jewish (ASJ) AF: 0.765 AC: 2653 AN: 3470

East Asian (EAS) AF: 0.605 AC: 3128 AN: 5172

South Asian (SAS) AF: 0.528 AC: 2547 AN: 4822

European-Finnish (FIN) AF: 0.767 AC: 8113 AN: 10572

Middle Eastern (MID) AF: 0.755 AC: 222 AN: 294

European-Non Finnish (NFE) AF: 0.752 AC: 51118 AN: 67962

Other (OTH) AF: 0.675 AC: 1428 AN: 2116

Alfa AF: 0.723 Hom.: 65788

Bravo AF: 0.645

Asia WGS AF: 0.556 AC: 1935 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.1
CADD	Benign	0.26
DANN	Benign	0.23
PhyloP100		-1.4

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs325648;

hg19: chr11-6204316;