rs10761571

Variant names:

• chr10-61147270-A-C
• rs10761571
• ENST00000687498.1:n.132-46702A>C

Your query was ambiguous. Multiple possible variants found:

• chr10-61147270-A-C
• chr10-61147270-A-G
• chr10-61147270-A-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000687498.1(LINC00845):​n.132-46702A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.587 in 151,952 control chromosomes in the GnomAD database, including 26,556 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 0.59 (26556 hom., cov: 33)
• Consequence: LINC00845 ENST00000687498.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.113

Genes affected

LINC00845 (HGNC:45033): (long intergenic non-protein coding RNA 845)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.725 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
LINC00845	ENST00000687498.1	n.132-46702A>C		intron_variant	Intron 1 of 1

Frequencies

GnomAD3 genomes AF: 0.587 AC: 89117 AN: 151834 Hom.: 26542 Cov.: 33

Gnomad AFR AF: 0.616

Gnomad AMI AF: 0.577

Gnomad AMR AF: 0.640

Gnomad ASJ AF: 0.533

Gnomad EAS AF: 0.745

Gnomad SAS AF: 0.669

Gnomad FIN AF: 0.401

Gnomad MID AF: 0.693

Gnomad NFE AF: 0.570

Gnomad OTH AF: 0.595

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

GnomAD4 genome AF: 0.587 AC: 89178 AN: 151952 Hom.: 26556 Cov.: 33 AF XY: 0.583 AC XY: 43275 AN XY: 74264

Gnomad4 AFR AF: 0.616

Gnomad4 AMR AF: 0.641

Gnomad4 ASJ AF: 0.533

Gnomad4 EAS AF: 0.745

Gnomad4 SAS AF: 0.669

Gnomad4 FIN AF: 0.401

Gnomad4 NFE AF: 0.570

Gnomad4 OTH AF: 0.597

Alfa AF: 0.584 Hom.: 20354

Bravo AF: 0.607

Asia WGS AF: 0.714 AC: 2481 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	5.9
DANN	Benign	0.67

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs10761571; hg19: chr10-62907028;