17-70330197-T-C

Variant names:

• chr17-70330197-T-C
• rs312691
• ENST00000592809.1:n.176+3319A>G

Variant summary

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

The ENST00000592809.1(ENSG00000267109):​n.176+3319A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.25 in 152,122 control chromosomes in the GnomAD database, including 4,961 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 0.25 (4961 hom., cov: 32)
• Consequence: ENSG00000267109 ENST00000592809.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.247
• Publications: 24 publications found

Genes affected

ENSG00000267109 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.453 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000592809.1. 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
	ENSG00000267109	ENST00000592809.1	TSL:3	n.176+3319A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.250 AC: 37970 AN: 152004 Hom.: 4949 Cov.: 32

Gnomad AFR AF: 0.245

Gnomad AMI AF: 0.276

Gnomad AMR AF: 0.298

Gnomad ASJ AF: 0.290

Gnomad EAS AF: 0.468

Gnomad SAS AF: 0.176

Gnomad FIN AF: 0.170

Gnomad MID AF: 0.307

Gnomad NFE AF: 0.241

Gnomad OTH AF: 0.244

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

GnomAD4 genome AF: 0.250 AC: 37999 AN: 152122 Hom.: 4961 Cov.: 32 AF XY: 0.248 AC XY: 18455 AN XY: 74362

African (AFR) AF: 0.245 AC: 10152 AN: 41518

American (AMR) AF: 0.298 AC: 4554 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.290 AC: 1005 AN: 3466

East Asian (EAS) AF: 0.469 AC: 2419 AN: 5158

South Asian (SAS) AF: 0.176 AC: 848 AN: 4828

European-Finnish (FIN) AF: 0.170 AC: 1798 AN: 10578

Middle Eastern (MID) AF: 0.306 AC: 90 AN: 294

European-Non Finnish (NFE) AF: 0.241 AC: 16367 AN: 67986

Other (OTH) AF: 0.244 AC: 515 AN: 2112

Alfa AF: 0.254 Hom.: 18942

Bravo AF: 0.265

Asia WGS AF: 0.311 AC: 1081 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	6.6
DANN	Benign	0.79
PhyloP100		0.25

Splicing

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

Other links and lift over

dbSNP: rs312691; hg19: chr17-68326338;