ENST00000665764.1:n.*109+22901C>T

Variant names:

• chr9-117995092-C-T
• rs2245960
• ENST00000665764.1:n.*109+22901C>T

Variant summary

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

The ENST00000665764.1(ENSG00000285082):​n.*109+22901C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.185 in 152,022 control chromosomes in the GnomAD database, including 2,754 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 0.19 (2754 hom., cov: 32)
• Consequence: ENSG00000285082 ENST00000665764.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.368
• Publications: 5 publications found

Genes affected

ENSG00000285082 (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 (NFE) allele frequency at 95% confidence interval = 0.195 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000665764.1. 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
	ENSG00000285082	ENST00000665764.1		n.*109+22901C>T		intron	N/A	ENSP00000499745.1	A0A2R8YGN2
	ENSG00000285082	ENST00000697636.1		n.*17-61938C>T		intron	N/A	ENSP00000513366.1	A0A2R8YGN2
	ENSG00000284977	ENST00000697639.1		n.1054-61938C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.185 AC: 28134 AN: 151904 Hom.: 2748 Cov.: 32

Gnomad AFR AF: 0.174

Gnomad AMI AF: 0.106

Gnomad AMR AF: 0.167

Gnomad ASJ AF: 0.354

Gnomad EAS AF: 0.0372

Gnomad SAS AF: 0.156

Gnomad FIN AF: 0.206

Gnomad MID AF: 0.282

Gnomad NFE AF: 0.198

Gnomad OTH AF: 0.196

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

GnomAD4 genome AF: 0.185 AC: 28154 AN: 152022 Hom.: 2754 Cov.: 32 AF XY: 0.184 AC XY: 13690 AN XY: 74284

African (AFR) AF: 0.174 AC: 7201 AN: 41450

American (AMR) AF: 0.166 AC: 2542 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.354 AC: 1227 AN: 3470

East Asian (EAS) AF: 0.0371 AC: 192 AN: 5174

South Asian (SAS) AF: 0.157 AC: 758 AN: 4818

European-Finnish (FIN) AF: 0.206 AC: 2171 AN: 10540

Middle Eastern (MID) AF: 0.272 AC: 80 AN: 294

European-Non Finnish (NFE) AF: 0.198 AC: 13465 AN: 67976

Other (OTH) AF: 0.199 AC: 421 AN: 2112

Alfa AF: 0.195 Hom.: 12594

Bravo AF: 0.181

Asia WGS AF: 0.101 AC: 351 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.9
DANN	Benign	0.71
PhyloP100		-0.37

Splicing

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

Other links and lift over

dbSNP: rs2245960; hg19: chr9-120757370;