chr5-165656790-C-T

Variant names:

• chr5-165656790-C-T
• rs262714
• ENST00000522189.1:n.22-121187C>T

Variant summary

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

The ENST00000522189.1(ENSG00000253693):​n.22-121187C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.674 in 152,030 control chromosomes in the GnomAD database, including 34,953 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 0.67 (34953 hom., cov: 32)
• Consequence: ENSG00000253693 ENST00000522189.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.172
• Publications: 3 publications found

Genes affected

ENSG00000253693 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.779 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000522189.1. 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
	ENSG00000253693	ENST00000522189.1	TSL:5	n.22-121187C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.674 AC: 102399 AN: 151912 Hom.: 34924 Cov.: 32

Gnomad AFR AF: 0.786

Gnomad AMI AF: 0.689

Gnomad AMR AF: 0.683

Gnomad ASJ AF: 0.629

Gnomad EAS AF: 0.726

Gnomad SAS AF: 0.627

Gnomad FIN AF: 0.662

Gnomad MID AF: 0.586

Gnomad NFE AF: 0.608

Gnomad OTH AF: 0.649

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

GnomAD4 genome AF: 0.674 AC: 102480 AN: 152030 Hom.: 34953 Cov.: 32 AF XY: 0.676 AC XY: 50226 AN XY: 74290

African (AFR) AF: 0.786 AC: 32619 AN: 41486

American (AMR) AF: 0.682 AC: 10428 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.629 AC: 2183 AN: 3470

East Asian (EAS) AF: 0.725 AC: 3726 AN: 5136

South Asian (SAS) AF: 0.627 AC: 3018 AN: 4814

European-Finnish (FIN) AF: 0.662 AC: 7006 AN: 10578

Middle Eastern (MID) AF: 0.599 AC: 175 AN: 292

European-Non Finnish (NFE) AF: 0.608 AC: 41338 AN: 67954

Other (OTH) AF: 0.645 AC: 1360 AN: 2110

Alfa AF: 0.631 Hom.: 43806

Bravo AF: 0.682

Asia WGS AF: 0.654 AC: 2274 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	8.3
DANN	Benign	0.67
PhyloP100		-0.17

Splicing

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

Other links and lift over

dbSNP: rs262714; hg19: chr5-165083795;