ENST00000598079.1:n.214-1352T>G

Variant names:

• chr19-50849559-T-G
• rs2569733
• ENST00000598079.1:n.214-1352T>G

Variant summary

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

The ENST00000598079.1(ENSG00000267968):​n.214-1352T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.206 in 152,160 control chromosomes in the GnomAD database, including 3,888 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 0.21 (3888 hom., cov: 32)
• Consequence: ENSG00000267968 ENST00000598079.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.106
• Publications: 5 publications found

Genes affected

ENSG00000267968 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.338 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LOC105372441	NR_131203.1	n.214-1352T>G		intron_variant	Intron 2 of 2
LOC105372441	NR_131205.1	n.231-1352T>G		intron_variant	Intron 2 of 2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ENSG00000267968	ENST00000598079.1	n.214-1352T>G		intron_variant	Intron 2 of 2	3

Frequencies

GnomAD3 genomes AF: 0.206 AC: 31320 AN: 152042 Hom.: 3885 Cov.: 32

Gnomad AFR AF: 0.0900

Gnomad AMI AF: 0.154

Gnomad AMR AF: 0.316

Gnomad ASJ AF: 0.232

Gnomad EAS AF: 0.352

Gnomad SAS AF: 0.149

Gnomad FIN AF: 0.331

Gnomad MID AF: 0.184

Gnomad NFE AF: 0.225

Gnomad OTH AF: 0.201

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

GnomAD4 genome AF: 0.206 AC: 31331 AN: 152160 Hom.: 3888 Cov.: 32 AF XY: 0.209 AC XY: 15576 AN XY: 74394

African (AFR) AF: 0.0899 AC: 3734 AN: 41534

American (AMR) AF: 0.316 AC: 4831 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.232 AC: 805 AN: 3466

East Asian (EAS) AF: 0.351 AC: 1813 AN: 5164

South Asian (SAS) AF: 0.148 AC: 714 AN: 4822

European-Finnish (FIN) AF: 0.331 AC: 3501 AN: 10580

Middle Eastern (MID) AF: 0.173 AC: 51 AN: 294

European-Non Finnish (NFE) AF: 0.225 AC: 15303 AN: 67992

Other (OTH) AF: 0.208 AC: 439 AN: 2112

Alfa AF: 0.219 Hom.: 520

Bravo AF: 0.202

Asia WGS AF: 0.266 AC: 926 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	3.6
DANN	Benign	0.50
PhyloP100		0.11

Splicing

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

Other links and lift over

dbSNP: rs2569733; hg19: chr19-51352815;