ENST00000673857.1:n.63-10882T>C

Variant names:

• chr6-31452241-T-C
• rs2516456
• ENST00000673857.1:n.63-10882T>C

Variant summary

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

The ENST00000673857.1(ENSG00000288587):​n.63-10882T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.511 in 151,592 control chromosomes in the GnomAD database, including 20,571 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 0.51 (20571 hom., cov: 31)
• Consequence: ENSG00000288587 ENST00000673857.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.40
• Publications: 5 publications found

Genes affected

ENSG00000288587 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.559 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000673857.1. 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
	ENSG00000288587	ENST00000673857.1		n.63-10882T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.511 AC: 77420 AN: 151474 Hom.: 20537 Cov.: 31

Gnomad AFR AF: 0.565

Gnomad AMI AF: 0.640

Gnomad AMR AF: 0.546

Gnomad ASJ AF: 0.563

Gnomad EAS AF: 0.210

Gnomad SAS AF: 0.437

Gnomad FIN AF: 0.494

Gnomad MID AF: 0.481

Gnomad NFE AF: 0.497

Gnomad OTH AF: 0.523

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

GnomAD4 genome AF: 0.511 AC: 77493 AN: 151592 Hom.: 20571 Cov.: 31 AF XY: 0.506 AC XY: 37494 AN XY: 74100

African (AFR) AF: 0.565 AC: 23305 AN: 41234

American (AMR) AF: 0.546 AC: 8270 AN: 15150

Ashkenazi Jewish (ASJ) AF: 0.563 AC: 1950 AN: 3464

East Asian (EAS) AF: 0.210 AC: 1086 AN: 5160

South Asian (SAS) AF: 0.439 AC: 2109 AN: 4804

European-Finnish (FIN) AF: 0.494 AC: 5207 AN: 10532

Middle Eastern (MID) AF: 0.469 AC: 134 AN: 286

European-Non Finnish (NFE) AF: 0.497 AC: 33759 AN: 67942

Other (OTH) AF: 0.517 AC: 1089 AN: 2108

Alfa AF: 0.503 Hom.: 22521

Bravo AF: 0.518

Asia WGS AF: 0.343 AC: 1191 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.9
DANN	Benign	0.55
PhyloP100		-1.4

Splicing

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

Other links and lift over

dbSNP: rs2516456; hg19: chr6-31420018;