chr8-124851782-A-T

Position:

• chr8-124851782-A-T

Variant summary

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

The ENST00000657463.1(LINC00964):​n.269+27812A>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 0.486 in 152,012 control chromosomes in the GnomAD database, including 18,216 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 0.49 (18216 hom., cov: 32)
• Consequence: LINC00964 ENST00000657463.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.51

Genes affected

LINC00964 (HGNC:27226): (long intergenic non-protein coding RNA 964)

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.644 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LOC105375743	XR_001745690.3	n.153+5581T>A		intron_variant, non_coding_transcript_variant
LOC105375743	XR_007061089.1	n.108+5355T>A		intron_variant, non_coding_transcript_variant
LOC105375743	XR_007061091.1	n.153+5581T>A		intron_variant, non_coding_transcript_variant
LOC105375743	XR_007061092.1	n.105+5355T>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LINC00964	ENST00000657463.1	n.269+27812A>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.486 AC: 73828 AN: 151894 Hom.: 18205 Cov.: 32

Gnomad AFR AF: 0.446

Gnomad AMI AF: 0.600

Gnomad AMR AF: 0.479

Gnomad ASJ AF: 0.494

Gnomad EAS AF: 0.663

Gnomad SAS AF: 0.517

Gnomad FIN AF: 0.454

Gnomad MID AF: 0.525

Gnomad NFE AF: 0.499

Gnomad OTH AF: 0.493

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

GnomAD4 genome AF: 0.486 AC: 73870 AN: 152012 Hom.: 18216 Cov.: 32 AF XY: 0.487 AC XY: 36144 AN XY: 74284

Gnomad4 AFR AF: 0.446

Gnomad4 AMR AF: 0.478

Gnomad4 ASJ AF: 0.494

Gnomad4 EAS AF: 0.663

Gnomad4 SAS AF: 0.518

Gnomad4 FIN AF: 0.454

Gnomad4 NFE AF: 0.499

Gnomad4 OTH AF: 0.500

Alfa AF: 0.349 Hom.: 864

Bravo AF: 0.482

Asia WGS AF: 0.603 AC: 2099 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	8.1
DANN	Benign	0.68

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs6470289; hg19: chr8-125864024;