ENST00000762810.1:n.739G>C

Variant names:

• chr5-4198261-G-C
• rs6555260
• ENST00000762810.1:n.739G>C

Variant summary

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

The ENST00000762810.1(ENSG00000299354):​n.739G>C variant causes a non coding transcript exon change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.923 in 152,180 control chromosomes in the GnomAD database, including 65,110 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 0.92 (65110 hom., cov: 30)
• Consequence: ENSG00000299354 ENST00000762810.1 non_coding_transcript_exon
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.393
• Publications: 1 publications found

Genes affected

ENSG00000299354 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.971 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000762810.1. 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
	ENSG00000299354	ENST00000762810.1		n.739G>C		non_coding_transcript_exon	Exon 3 of 3

Frequencies

GnomAD3 genomes AF: 0.923 AC: 140357 AN: 152062 Hom.: 65086 Cov.: 30

Gnomad AFR AF: 0.831

Gnomad AMI AF: 0.959

Gnomad AMR AF: 0.953

Gnomad ASJ AF: 0.969

Gnomad EAS AF: 0.994

Gnomad SAS AF: 0.901

Gnomad FIN AF: 0.985

Gnomad MID AF: 0.949

Gnomad NFE AF: 0.955

Gnomad OTH AF: 0.926

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

GnomAD4 genome AF: 0.923 AC: 140433 AN: 152180 Hom.: 65110 Cov.: 30 AF XY: 0.924 AC XY: 68745 AN XY: 74390

African (AFR) AF: 0.831 AC: 34490 AN: 41492

American (AMR) AF: 0.953 AC: 14586 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.969 AC: 3363 AN: 3472

East Asian (EAS) AF: 0.994 AC: 5119 AN: 5150

South Asian (SAS) AF: 0.901 AC: 4340 AN: 4818

European-Finnish (FIN) AF: 0.985 AC: 10437 AN: 10598

Middle Eastern (MID) AF: 0.956 AC: 281 AN: 294

European-Non Finnish (NFE) AF: 0.955 AC: 65000 AN: 68028

Other (OTH) AF: 0.918 AC: 1942 AN: 2116

Alfa AF: 0.675 Hom.: 155

Bravo AF: 0.919

Asia WGS AF: 0.912 AC: 3171 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	4.4
DANN	Benign	0.47
PhyloP100		-0.39

Splicing

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

Other links and lift over

dbSNP: rs6555260; hg19: chr5-4198374;