chr15-39023157-G-C

Variant names:

• chr15-39023157-G-C
• rs12907914
• ENST00000560197.6:n.170+48346C>G

Variant summary

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

The ENST00000560197.6(ENSG00000259345):​n.170+48346C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.302 in 152,090 control chromosomes in the GnomAD database, including 7,671 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 (7671 hom., cov: 32)
• Consequence: ENSG00000259345 ENST00000560197.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.283
• Publications: 8 publications found

Genes affected

ENSG00000259345 (HGNC:):

LINC02694 (HGNC:33796): (long intergenic non-protein coding RNA 2694)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.368 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LOC105370781	NR_188221.1	n.90-1056G>C		intron_variant	Intron 1 of 2
LOC105370777	XR_007064586.1	n.1445+48346C>G		intron_variant	Intron 3 of 4
LOC105370777	XR_007064587.1	n.1445+48346C>G		intron_variant	Intron 3 of 4
LOC105370777	XR_007064588.1	n.623+48346C>G		intron_variant	Intron 2 of 3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ENSG00000259345	ENST00000560197.6	n.170+48346C>G		intron_variant	Intron 2 of 7	5
ENSG00000259345	ENST00000560484.1	n.173+48346C>G		intron_variant	Intron 2 of 3	4
ENSG00000259278	ENST00000560709.1	n.93-997G>C		intron_variant	Intron 1 of 2	4

Frequencies

GnomAD3 genomes AF: 0.302 AC: 45926 AN: 151972 Hom.: 7669 Cov.: 32

Gnomad AFR AF: 0.154

Gnomad AMI AF: 0.474

Gnomad AMR AF: 0.344

Gnomad ASJ AF: 0.334

Gnomad EAS AF: 0.342

Gnomad SAS AF: 0.319

Gnomad FIN AF: 0.313

Gnomad MID AF: 0.358

Gnomad NFE AF: 0.372

Gnomad OTH AF: 0.316

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

GnomAD4 genome AF: 0.302 AC: 45934 AN: 152090 Hom.: 7671 Cov.: 32 AF XY: 0.301 AC XY: 22377 AN XY: 74376

African (AFR) AF: 0.154 AC: 6385 AN: 41498

American (AMR) AF: 0.344 AC: 5253 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.334 AC: 1159 AN: 3470

East Asian (EAS) AF: 0.341 AC: 1763 AN: 5166

South Asian (SAS) AF: 0.319 AC: 1541 AN: 4828

European-Finnish (FIN) AF: 0.313 AC: 3313 AN: 10586

Middle Eastern (MID) AF: 0.374 AC: 110 AN: 294

European-Non Finnish (NFE) AF: 0.372 AC: 25300 AN: 67960

Other (OTH) AF: 0.322 AC: 679 AN: 2110

Alfa AF: 0.221 Hom.: 522

Bravo AF: 0.296

Asia WGS AF: 0.341 AC: 1184 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	1.1
DANN	Benign	0.42
PhyloP100		-0.28

Splicing

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

Other links and lift over

dbSNP: rs12907914; hg19: chr15-39315358;