rs6951656

chr7-91403759-A-Cchr7-91403759-A-Gchr7-91403759-A-T

Variant summary

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

The NR_183366.1(LINC02932):n.244-63086A>C variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.41 in 151,292 control chromosomes in the GnomAD database, including 15,144 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 0.41 (15144 hom., cov: 31)
• Consequence: LINC02932 NR_183366.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0150

Genes affected

LINC02932 (HGNC:55875): (long intergenic non-protein coding RNA 2932)

(HGNC:):

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 = 0.546 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LINC02932	NR_183366.1	n.244-63086A>C		intron_variant, non_coding_transcript_variant
LINC02932	NR_183367.1	n.244-63086A>C		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LINC02932	ENST00000418395.1	n.182-63086A>C		intron_variant, non_coding_transcript_variant		3
	ENST00000456952.1	n.113-22892T>G		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.410 AC: 61960 AN: 151168 Hom.: 15144 Cov.: 31

Gnomad AFR AF: 0.168

Gnomad AMI AF: 0.477

Gnomad AMR AF: 0.376

Gnomad ASJ AF: 0.521

Gnomad EAS AF: 0.245

Gnomad SAS AF: 0.345

Gnomad FIN AF: 0.548

Gnomad MID AF: 0.583

Gnomad NFE AF: 0.551

Gnomad OTH AF: 0.445

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

GnomAD4 genome AF: 0.410 AC: 61956 AN: 151292 Hom.: 15144 Cov.: 31 AF XY: 0.407 AC XY: 30027 AN XY: 73856

Gnomad4 AFR AF: 0.168

Gnomad4 AMR AF: 0.375

Gnomad4 ASJ AF: 0.521

Gnomad4 EAS AF: 0.245

Gnomad4 SAS AF: 0.348

Gnomad4 FIN AF: 0.548

Gnomad4 NFE AF: 0.551

Gnomad4 OTH AF: 0.440

Alfa AF: 0.520 Hom.: 17059

Bravo AF: 0.388

Asia WGS AF: 0.263 AC: 907 AN: 3436

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
Cadd	Benign	1.4
Dann	Benign	0.76

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs6951656; hg19: chr7-91033074;