chr3-107507158-A-T

Variant names:

• chr3-107507158-A-T
• rs618213

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 0.128 in 152,212 control chromosomes in the GnomAD database, including 1,409 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 0.13 (1409 hom., cov: 32)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0880

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.151 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: 0.128 AC: 19446 AN: 152094 Hom.: 1409 Cov.: 32

Gnomad AFR AF: 0.107

Gnomad AMI AF: 0.0230

Gnomad AMR AF: 0.0932

Gnomad ASJ AF: 0.107

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.0521

Gnomad FIN AF: 0.215

Gnomad MID AF: 0.0475

Gnomad NFE AF: 0.153

Gnomad OTH AF: 0.113

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

GnomAD4 genome AF: 0.128 AC: 19450 AN: 152212 Hom.: 1409 Cov.: 32 AF XY: 0.127 AC XY: 9446 AN XY: 74414

Gnomad4 AFR AF: 0.107

Gnomad4 AMR AF: 0.0931

Gnomad4 ASJ AF: 0.107

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.0525

Gnomad4 FIN AF: 0.215

Gnomad4 NFE AF: 0.153

Gnomad4 OTH AF: 0.112

Alfa AF: 0.0874 Hom.: 133

Bravo AF: 0.119

Asia WGS AF: 0.0310 AC: 108 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	8.2
DANN	Benign	0.57

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs618213; hg19: chr3-107226005; COSMIC: COSV69624968;