ENST00000672708.1:n.294+746C>T

Variant names:

• chr10-117590250-C-T
• rs71003
• ENST00000672708.1:n.294+746C>T

Variant summary

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

The ENST00000672708.1(ENSG00000288172):​n.294+746C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.61 in 149,644 control chromosomes in the GnomAD database, including 27,849 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 0.61 (27849 hom., cov: 25)
• Consequence: ENSG00000288172 ENST00000672708.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.341
• Publications: 1 publications found

Genes affected

ENSG00000288172 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.656 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000672708.1. 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
	ENSG00000288172	ENST00000672708.1		n.294+746C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.609 AC: 91130 AN: 149530 Hom.: 27806 Cov.: 25

Gnomad AFR AF: 0.616

Gnomad AMI AF: 0.680

Gnomad AMR AF: 0.608

Gnomad ASJ AF: 0.671

Gnomad EAS AF: 0.539

Gnomad SAS AF: 0.677

Gnomad FIN AF: 0.645

Gnomad MID AF: 0.612

Gnomad NFE AF: 0.598

Gnomad OTH AF: 0.576

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

GnomAD4 genome AF: 0.610 AC: 91240 AN: 149644 Hom.: 27849 Cov.: 25 AF XY: 0.615 AC XY: 44746 AN XY: 72816

African (AFR) AF: 0.616 AC: 24982 AN: 40530

American (AMR) AF: 0.608 AC: 9122 AN: 14994

Ashkenazi Jewish (ASJ) AF: 0.671 AC: 2325 AN: 3466

East Asian (EAS) AF: 0.540 AC: 2704 AN: 5010

South Asian (SAS) AF: 0.676 AC: 3186 AN: 4716

European-Finnish (FIN) AF: 0.645 AC: 6482 AN: 10056

Middle Eastern (MID) AF: 0.600 AC: 174 AN: 290

European-Non Finnish (NFE) AF: 0.598 AC: 40450 AN: 67610

Other (OTH) AF: 0.580 AC: 1199 AN: 2066

Alfa AF: 0.595 Hom.: 45640

Bravo AF: 0.600

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.54
DANN	Benign	0.57
PhyloP100		-0.34

Splicing

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

Other links and lift over

dbSNP: rs71003; hg19: chr10-119349761;