6-166957622-T-C

Variant names:

• chr6-166957622-T-C
• rs2149085

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 0.576 in 152,226 control chromosomes in the GnomAD database, including 26,319 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 0.58 (26319 hom., cov: 34)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.72

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.73 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: 0.576 AC: 87622 AN: 152108 Hom.: 26266 Cov.: 34

Gnomad AFR AF: 0.736

Gnomad AMI AF: 0.564

Gnomad AMR AF: 0.611

Gnomad ASJ AF: 0.527

Gnomad EAS AF: 0.622

Gnomad SAS AF: 0.695

Gnomad FIN AF: 0.533

Gnomad MID AF: 0.544

Gnomad NFE AF: 0.468

Gnomad OTH AF: 0.584

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

GnomAD4 genome AF: 0.576 AC: 87733 AN: 152226 Hom.: 26319 Cov.: 34 AF XY: 0.582 AC XY: 43288 AN XY: 74432

Gnomad4 AFR AF: 0.737

Gnomad4 AMR AF: 0.611

Gnomad4 ASJ AF: 0.527

Gnomad4 EAS AF: 0.621

Gnomad4 SAS AF: 0.696

Gnomad4 FIN AF: 0.533

Gnomad4 NFE AF: 0.468

Gnomad4 OTH AF: 0.588

Alfa AF: 0.531 Hom.: 3746

Bravo AF: 0.591

Asia WGS AF: 0.667 AC: 2318 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	1.0
DANN	Benign	0.38

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs2149085; hg19: chr6-167371110;