5-135911101-G-A

Variant names:

• chr5-135911101-G-A
• rs12522916
• ENST00000523722.1:n.240-1279C>T

Variant summary

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

The ENST00000523722.1(ENSG00000253927):​n.240-1279C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.18 in 152,180 control chromosomes in the GnomAD database, including 2,670 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 0.18 (2670 hom., cov: 32)
• Consequence: ENSG00000253927 ENST00000523722.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.356
• Publications: 1 publications found

Genes affected

ENSG00000253927 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.244 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000523722.1. 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
	ENSG00000253927	ENST00000523722.1	TSL:3	n.240-1279C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.181 AC: 27448 AN: 152062 Hom.: 2666 Cov.: 32

Gnomad AFR AF: 0.106

Gnomad AMI AF: 0.217

Gnomad AMR AF: 0.186

Gnomad ASJ AF: 0.202

Gnomad EAS AF: 0.255

Gnomad SAS AF: 0.188

Gnomad FIN AF: 0.183

Gnomad MID AF: 0.234

Gnomad NFE AF: 0.216

Gnomad OTH AF: 0.201

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

GnomAD4 genome AF: 0.180 AC: 27455 AN: 152180 Hom.: 2670 Cov.: 32 AF XY: 0.181 AC XY: 13428 AN XY: 74384

African (AFR) AF: 0.106 AC: 4388 AN: 41540

American (AMR) AF: 0.185 AC: 2835 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.202 AC: 700 AN: 3470

East Asian (EAS) AF: 0.255 AC: 1319 AN: 5168

South Asian (SAS) AF: 0.188 AC: 905 AN: 4814

European-Finnish (FIN) AF: 0.183 AC: 1936 AN: 10580

Middle Eastern (MID) AF: 0.231 AC: 68 AN: 294

European-Non Finnish (NFE) AF: 0.216 AC: 14687 AN: 67996

Other (OTH) AF: 0.198 AC: 420 AN: 2116

Alfa AF: 0.207 Hom.: 1955

Bravo AF: 0.178

Asia WGS AF: 0.220 AC: 766 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	2.4
DANN	Benign	0.32
PhyloP100		-0.36

Splicing

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

Other links and lift over

dbSNP: rs12522916; hg19: chr5-135246790;