rs10496060

Variant names:

• chr2-56987948-T-A
• rs10496060

Your query was ambiguous. Multiple possible variants found:

• chr2-56987948-T-A
• chr2-56987948-T-C
• chr2-56987948-T-G

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 0.103 in 152,210 control chromosomes in the GnomAD database, including 2,139 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 0.10 (2139 hom., cov: 33)
• Consequence: Unknown
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0770

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 (EAS) allele frequency at 95% confidence interval = 0.399 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: 0.103 AC: 15619 AN: 152092 Hom.: 2136 Cov.: 33

Gnomad AFR AF: 0.280

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0472

Gnomad ASJ AF: 0.0138

Gnomad EAS AF: 0.415

Gnomad SAS AF: 0.0387

Gnomad FIN AF: 0.0128

Gnomad MID AF: 0.0316

Gnomad NFE AF: 0.00882

Gnomad OTH AF: 0.0860

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

GnomAD4 genome AF: 0.103 AC: 15644 AN: 152210 Hom.: 2139 Cov.: 33 AF XY: 0.104 AC XY: 7706 AN XY: 74406

Gnomad4 AFR AF: 0.280

Gnomad4 AMR AF: 0.0472

Gnomad4 ASJ AF: 0.0138

Gnomad4 EAS AF: 0.414

Gnomad4 SAS AF: 0.0385

Gnomad4 FIN AF: 0.0128

Gnomad4 NFE AF: 0.00882

Gnomad4 OTH AF: 0.0847

Alfa AF: 0.0647 Hom.: 131

Bravo AF: 0.116

Asia WGS AF: 0.193 AC: 670 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	4.6
DANN	Benign	0.74

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs10496060; hg19: chr2-57215083;