chr13-94744403-G-A

Variant names:

• chr13-94744403-G-A
• rs12874914
• ENST00000665450.1:n.133-20005G>A

Variant summary

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

The ENST00000665450.1(SOX21-AS1):​n.133-20005G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.196 in 151,908 control chromosomes in the GnomAD database, including 3,362 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 0.20 (3362 hom., cov: 31)
• Consequence: SOX21-AS1 ENST00000665450.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.493
• Publications: 2 publications found

Genes affected

SOX21-AS1 (HGNC:39807): (SOX21 antisense divergent transcript 1)

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 (SAS) allele frequency at 95% confidence interval = 0.377 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000665450.1. 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
	SOX21-AS1	ENST00000665450.1		n.133-20005G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.197 AC: 29841 AN: 151790 Hom.: 3361 Cov.: 31

Gnomad AFR AF: 0.105

Gnomad AMI AF: 0.0636

Gnomad AMR AF: 0.202

Gnomad ASJ AF: 0.131

Gnomad EAS AF: 0.350

Gnomad SAS AF: 0.393

Gnomad FIN AF: 0.238

Gnomad MID AF: 0.0759

Gnomad NFE AF: 0.225

Gnomad OTH AF: 0.193

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

GnomAD4 genome AF: 0.196 AC: 29849 AN: 151908 Hom.: 3362 Cov.: 31 AF XY: 0.200 AC XY: 14845 AN XY: 74202

African (AFR) AF: 0.105 AC: 4341 AN: 41446

American (AMR) AF: 0.201 AC: 3077 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.131 AC: 453 AN: 3466

East Asian (EAS) AF: 0.349 AC: 1798 AN: 5152

South Asian (SAS) AF: 0.392 AC: 1872 AN: 4774

European-Finnish (FIN) AF: 0.238 AC: 2511 AN: 10538

Middle Eastern (MID) AF: 0.0850 AC: 25 AN: 294

European-Non Finnish (NFE) AF: 0.225 AC: 15301 AN: 67942

Other (OTH) AF: 0.196 AC: 413 AN: 2104

Alfa AF: 0.197 Hom.: 421

Bravo AF: 0.186

Asia WGS AF: 0.369 AC: 1281 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	0.88
DANN	Benign	0.52
PhyloP100		-0.49

Splicing

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

Other links and lift over

dbSNP: rs12874914; hg19: chr13-95396657;