rs897876

Variant names:

• chr2-65564447-C-T
• rs897876
• ENST00000377977.3:n.862+63300C>T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000377977.3(LINC02934):​n.862+63300C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.301 in 152,118 control chromosomes in the GnomAD database, including 7,060 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 0.30 (7060 hom., cov: 32)
• Consequence: LINC02934 ENST00000377977.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.579
• Publications: 2 publications found

Genes affected

LINC02934 (HGNC:55913): (long intergenic non-protein coding RNA 2934)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.377 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000377977.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINC02934	ENST00000377977.3	TSL:2	n.862+63300C>T		intron	N/A
	LINC02934	ENST00000606978.5	TSL:5	n.455+81295C>T		intron	N/A
	LINC02934	ENST00000822260.1		n.367+81295C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.301 AC: 45763 AN: 152000 Hom.: 7056 Cov.: 32

Gnomad AFR AF: 0.301

Gnomad AMI AF: 0.295

Gnomad AMR AF: 0.252

Gnomad ASJ AF: 0.261

Gnomad EAS AF: 0.392

Gnomad SAS AF: 0.175

Gnomad FIN AF: 0.331

Gnomad MID AF: 0.277

Gnomad NFE AF: 0.312

Gnomad OTH AF: 0.304

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

GnomAD4 genome AF: 0.301 AC: 45788 AN: 152118 Hom.: 7060 Cov.: 32 AF XY: 0.301 AC XY: 22384 AN XY: 74354

African (AFR) AF: 0.301 AC: 12491 AN: 41496

American (AMR) AF: 0.251 AC: 3841 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.261 AC: 906 AN: 3468

East Asian (EAS) AF: 0.392 AC: 2024 AN: 5168

South Asian (SAS) AF: 0.174 AC: 841 AN: 4824

European-Finnish (FIN) AF: 0.331 AC: 3498 AN: 10572

Middle Eastern (MID) AF: 0.281 AC: 82 AN: 292

European-Non Finnish (NFE) AF: 0.312 AC: 21193 AN: 67982

Other (OTH) AF: 0.304 AC: 643 AN: 2112

Alfa AF: 0.304 Hom.: 31149

Bravo AF: 0.292

Asia WGS AF: 0.255 AC: 886 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	1.8
DANN	Benign	0.58
PhyloP100		-0.58

Splicing

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

Other links and lift over

dbSNP: rs897876; hg19: chr2-65791581;