X-17992789-G-T

Position:

• chrX-17992789-G-T

Variant summary

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

The NR_133641.1(LINC01456):​n.194+3000C>A 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 0.268 in 110,913 control chromosomes in the GnomAD database, including 6,835 homozygotes. There are 8,487 hemizygotes in GnomAD. 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 0.27 (6835 hom., 8487 hem., cov: 22)
• Consequence: LINC01456 NR_133641.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.353

Genes affected

LINC01456 (HGNC:50846): (long intergenic non-protein coding RNA 1456)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.753 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LINC01456	NR_133641.1	n.194+3000C>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LINC01456	ENST00000453902.1	n.194+3000C>A		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.268 AC: 29668 AN: 110863 Hom.: 6833 Cov.: 22 AF XY: 0.255 AC XY: 8443 AN XY: 33099

Gnomad AFR AF: 0.761

Gnomad AMI AF: 0.0102

Gnomad AMR AF: 0.217

Gnomad ASJ AF: 0.0743

Gnomad EAS AF: 0.226

Gnomad SAS AF: 0.173

Gnomad FIN AF: 0.0779

Gnomad MID AF: 0.129

Gnomad NFE AF: 0.0404

Gnomad OTH AF: 0.248

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

GnomAD4 genome AF: 0.268 AC: 29722 AN: 110913 Hom.: 6835 Cov.: 22 AF XY: 0.256 AC XY: 8487 AN XY: 33159

Gnomad4 AFR AF: 0.761

Gnomad4 AMR AF: 0.217

Gnomad4 ASJ AF: 0.0743

Gnomad4 EAS AF: 0.226

Gnomad4 SAS AF: 0.173

Gnomad4 FIN AF: 0.0779

Gnomad4 NFE AF: 0.0404

Gnomad4 OTH AF: 0.246

Alfa AF: 0.177 Hom.: 1673

Bravo AF: 0.305

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	1.2
DANN	Benign	0.29

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs17320692; hg19: chrX-18010909;