chr17-50845301-C-T

Variant names:

• chr17-50845301-C-T
• rs12941977

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 0.133 in 152,260 control chromosomes in the GnomAD database, including 1,671 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 (1671 hom., cov: 32)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.20

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.185 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: 0.134 AC: 20327 AN: 152142 Hom.: 1674 Cov.: 32

Gnomad AFR AF: 0.0472

Gnomad AMI AF: 0.268

Gnomad AMR AF: 0.130

Gnomad ASJ AF: 0.201

Gnomad EAS AF: 0.000579

Gnomad SAS AF: 0.0820

Gnomad FIN AF: 0.177

Gnomad MID AF: 0.180

Gnomad NFE AF: 0.188

Gnomad OTH AF: 0.159

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

GnomAD4 genome AF: 0.133 AC: 20321 AN: 152260 Hom.: 1671 Cov.: 32 AF XY: 0.130 AC XY: 9688 AN XY: 74446

Gnomad4 AFR AF: 0.0470

Gnomad4 AMR AF: 0.130

Gnomad4 ASJ AF: 0.201

Gnomad4 EAS AF: 0.000580

Gnomad4 SAS AF: 0.0820

Gnomad4 FIN AF: 0.177

Gnomad4 NFE AF: 0.188

Gnomad4 OTH AF: 0.158

Alfa AF: 0.174 Hom.: 2405

Bravo AF: 0.127

Asia WGS AF: 0.0420 AC: 145 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	0.16
DANN	Benign	0.50

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs12941977; hg19: chr17-48922662;