rs11908586

Variant names:

• chr20-51152677-G-A
• rs11908586

Your query was ambiguous. Multiple possible variants found:

• chr20-51152677-G-A
• chr20-51152677-G-T

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 0.142 in 152,104 control chromosomes in the GnomAD database, including 2,645 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 0.14 (2645 hom., cov: 33)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.59

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.04).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.322 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: 0.142 AC: 21614 AN: 151986 Hom.: 2627 Cov.: 33

Gnomad AFR AF: 0.326

Gnomad AMI AF: 0.0866

Gnomad AMR AF: 0.0734

Gnomad ASJ AF: 0.162

Gnomad EAS AF: 0.0152

Gnomad SAS AF: 0.0816

Gnomad FIN AF: 0.0810

Gnomad MID AF: 0.0854

Gnomad NFE AF: 0.0700

Gnomad OTH AF: 0.131

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

GnomAD4 genome AF: 0.142 AC: 21670 AN: 152104 Hom.: 2645 Cov.: 33 AF XY: 0.139 AC XY: 10325 AN XY: 74374

Gnomad4 AFR AF: 0.326

Gnomad4 AMR AF: 0.0731

Gnomad4 ASJ AF: 0.162

Gnomad4 EAS AF: 0.0154

Gnomad4 SAS AF: 0.0810

Gnomad4 FIN AF: 0.0810

Gnomad4 NFE AF: 0.0700

Gnomad4 OTH AF: 0.134

Alfa AF: 0.0548 Hom.: 85

Bravo AF: 0.149

Asia WGS AF: 0.0850 AC: 298 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	1.8
DANN	Benign	0.52

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs11908586; hg19: chr20-49769214;