chr11-82608305-A-G

Variant names:

• chr11-82608305-A-G
• rs2186690
• ENST00000527364.2:n.485+1708T>C

Variant summary

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

The ENST00000527364.2(ENSG00000255246):​n.485+1708T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.911 in 152,158 control chromosomes in the GnomAD database, including 63,208 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 0.91 (63208 hom., cov: 33)
• Consequence: ENSG00000255246 ENST00000527364.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.356
• Publications: 1 publications found

Genes affected

ENSG00000255246 (HGNC:):

MIR4300HG (HGNC:52003): (MIR4300 host gene)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.968 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000527364.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000255246	ENST00000527364.2	TSL:3	n.485+1708T>C		intron	N/A
	MIR4300HG	ENST00000532217.1	TSL:5	n.440+64787T>C		intron	N/A
	ENSG00000255246	ENST00000661021.1		n.402-4204T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.911 AC: 138497 AN: 152040 Hom.: 63138 Cov.: 33

Gnomad AFR AF: 0.938

Gnomad AMI AF: 0.859

Gnomad AMR AF: 0.906

Gnomad ASJ AF: 0.893

Gnomad EAS AF: 0.991

Gnomad SAS AF: 0.836

Gnomad FIN AF: 0.933

Gnomad MID AF: 0.899

Gnomad NFE AF: 0.892

Gnomad OTH AF: 0.919

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

GnomAD4 genome AF: 0.911 AC: 138625 AN: 152158 Hom.: 63208 Cov.: 33 AF XY: 0.911 AC XY: 67792 AN XY: 74390

African (AFR) AF: 0.939 AC: 38985 AN: 41536

American (AMR) AF: 0.907 AC: 13834 AN: 15258

Ashkenazi Jewish (ASJ) AF: 0.893 AC: 3102 AN: 3472

East Asian (EAS) AF: 0.991 AC: 5130 AN: 5178

South Asian (SAS) AF: 0.836 AC: 4029 AN: 4820

European-Finnish (FIN) AF: 0.933 AC: 9900 AN: 10610

Middle Eastern (MID) AF: 0.908 AC: 267 AN: 294

European-Non Finnish (NFE) AF: 0.892 AC: 60651 AN: 67964

Other (OTH) AF: 0.920 AC: 1944 AN: 2114

Alfa AF: 0.912 Hom.: 28550

Bravo AF: 0.914

Asia WGS AF: 0.921 AC: 3197 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	1.2
DANN	Benign	0.54
PhyloP100		-0.36

Splicing

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

Other links and lift over

dbSNP: rs2186690; hg19: chr11-82319347;