ENST00000521685.5:n.167-6836C>A

Variant names:

• chr8-71169443-C-A
• rs7819928
• ENST00000521685.5:n.167-6836C>A

Variant summary

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

The ENST00000521685.5(ENSG00000254031):​n.167-6836C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.293 in 151,984 control chromosomes in the GnomAD database, including 9,272 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 0.29 (9272 hom., cov: 32)
• Consequence: ENSG00000254031 ENST00000521685.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.66
• Publications: 0 publications found

Genes affected

ENSG00000254031 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.04).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.589 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000521685.5. 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
	ENSG00000254031	ENST00000521685.5	TSL:3	n.167-6836C>A		intron	N/A
	ENSG00000285579	ENST00000647843.1		n.588-29697C>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.292 AC: 44388 AN: 151866 Hom.: 9243 Cov.: 32

Gnomad AFR AF: 0.595

Gnomad AMI AF: 0.193

Gnomad AMR AF: 0.163

Gnomad ASJ AF: 0.230

Gnomad EAS AF: 0.0991

Gnomad SAS AF: 0.307

Gnomad FIN AF: 0.172

Gnomad MID AF: 0.149

Gnomad NFE AF: 0.177

Gnomad OTH AF: 0.243

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

GnomAD4 genome AF: 0.293 AC: 44462 AN: 151984 Hom.: 9272 Cov.: 32 AF XY: 0.288 AC XY: 21430 AN XY: 74292

African (AFR) AF: 0.595 AC: 24656 AN: 41442

American (AMR) AF: 0.162 AC: 2480 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.230 AC: 799 AN: 3470

East Asian (EAS) AF: 0.0990 AC: 511 AN: 5162

South Asian (SAS) AF: 0.306 AC: 1474 AN: 4814

European-Finnish (FIN) AF: 0.172 AC: 1819 AN: 10576

Middle Eastern (MID) AF: 0.153 AC: 45 AN: 294

European-Non Finnish (NFE) AF: 0.177 AC: 11994 AN: 67926

Other (OTH) AF: 0.240 AC: 508 AN: 2114

Alfa AF: 0.204 Hom.: 6666

Bravo AF: 0.301

Asia WGS AF: 0.225 AC: 780 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.097
DANN	Benign	0.40
PhyloP100		-1.7

Splicing

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

Other links and lift over

dbSNP: rs7819928; hg19: chr8-72081678;