chr3-12439876-C-T

Variant names:

• chr3-12439876-C-T
• rs4498025

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The variant allele was found at a frequency of 0.188 in 152,062 control chromosomes in the GnomAD database, including 3,417 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 (3417 hom., cov: 31)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.724

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.256 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt

Frequencies

GnomAD3 genomes AF: 0.188 AC: 28536 AN: 151944 Hom.: 3420 Cov.: 31

Gnomad AFR AF: 0.0490

Gnomad AMI AF: 0.390

Gnomad AMR AF: 0.188

Gnomad ASJ AF: 0.264

Gnomad EAS AF: 0.125

Gnomad SAS AF: 0.128

Gnomad FIN AF: 0.287

Gnomad MID AF: 0.241

Gnomad NFE AF: 0.259

Gnomad OTH AF: 0.179

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

GnomAD4 genome AF: 0.188 AC: 28528 AN: 152062 Hom.: 3417 Cov.: 31 AF XY: 0.188 AC XY: 13978 AN XY: 74326

Gnomad4 AFR AF: 0.0490

Gnomad4 AMR AF: 0.188

Gnomad4 ASJ AF: 0.264

Gnomad4 EAS AF: 0.125

Gnomad4 SAS AF: 0.128

Gnomad4 FIN AF: 0.287

Gnomad4 NFE AF: 0.259

Gnomad4 OTH AF: 0.177

Alfa AF: 0.232 Hom.: 6224

Bravo AF: 0.175

Asia WGS AF: 0.141 AC: 492 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.76
DANN	Benign	0.75

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs4498025; hg19: chr3-12481375;