chr13-37937078-C-T

Position:

• chr13-37937078-C-T

Variant summary

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

The ENST00000667295.1(LINC02334):​n.442+2041C>T 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 0.428 in 151,976 control chromosomes in the GnomAD database, including 14,818 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 0.43 (14818 hom., cov: 32)
• Consequence: LINC02334 ENST00000667295.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.455

Genes affected

LINC02334 (HGNC:53254): (long intergenic non-protein coding RNA 2334)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.52 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
LINC02334	XR_941880.4	n.590+2041C>T		intron_variant, non_coding_transcript_variant
LINC02334	XR_941877.3	n.590+2041C>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
LINC02334	ENST00000667295.1	n.442+2041C>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.428 AC: 64979 AN: 151858 Hom.: 14819 Cov.: 32

Gnomad AFR AF: 0.322

Gnomad AMI AF: 0.561

Gnomad AMR AF: 0.376

Gnomad ASJ AF: 0.512

Gnomad EAS AF: 0.128

Gnomad SAS AF: 0.380

Gnomad FIN AF: 0.416

Gnomad MID AF: 0.446

Gnomad NFE AF: 0.525

Gnomad OTH AF: 0.447

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

GnomAD4 genome AF: 0.428 AC: 64991 AN: 151976 Hom.: 14818 Cov.: 32 AF XY: 0.419 AC XY: 31088 AN XY: 74228

Gnomad4 AFR AF: 0.322

Gnomad4 AMR AF: 0.376

Gnomad4 ASJ AF: 0.512

Gnomad4 EAS AF: 0.128

Gnomad4 SAS AF: 0.380

Gnomad4 FIN AF: 0.416

Gnomad4 NFE AF: 0.525

Gnomad4 OTH AF: 0.442

Alfa AF: 0.514 Hom.: 36716

Bravo AF: 0.420

Asia WGS AF: 0.238 AC: 827 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.1
DANN	Benign	0.56

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1337604; hg19: chr13-38511215;