rs9866825

chr3-8209103-A-Cchr3-8209103-A-Gchr3-8209103-A-T

Variant summary

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

The ENST00000654635.1(LMCD1-AS1):n.589-14030T>G 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 0.564 in 152,016 control chromosomes in the GnomAD database, including 24,403 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 0.56 (24403 hom., cov: 32)
• Consequence: LMCD1-AS1 ENST00000654635.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.278

Genes affected

LMCD1-AS1 (HGNC:44477): (LMCD1 antisense RNA 1)

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.738 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LMCD1-AS1	ENST00000654635.1	n.589-14030T>G		intron_variant, non_coding_transcript_variant
LMCD1-AS1	ENST00000446281.5	n.515-216801T>G		intron_variant, non_coding_transcript_variant		5
LMCD1-AS1	ENST00000452802.6	n.583-14030T>G		intron_variant, non_coding_transcript_variant		2
LMCD1-AS1	ENST00000659617.1	n.597-14030T>G		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.564 AC: 85663 AN: 151898 Hom.: 24371 Cov.: 32

Gnomad AFR AF: 0.598

Gnomad AMI AF: 0.592

Gnomad AMR AF: 0.527

Gnomad ASJ AF: 0.477

Gnomad EAS AF: 0.758

Gnomad SAS AF: 0.675

Gnomad FIN AF: 0.589

Gnomad MID AF: 0.583

Gnomad NFE AF: 0.529

Gnomad OTH AF: 0.556

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

GnomAD4 genome AF: 0.564 AC: 85743 AN: 152016 Hom.: 24403 Cov.: 32 AF XY: 0.569 AC XY: 42254 AN XY: 74304

Gnomad4 AFR AF: 0.598

Gnomad4 AMR AF: 0.527

Gnomad4 ASJ AF: 0.477

Gnomad4 EAS AF: 0.758

Gnomad4 SAS AF: 0.676

Gnomad4 FIN AF: 0.589

Gnomad4 NFE AF: 0.529

Gnomad4 OTH AF: 0.560

Alfa AF: 0.548 Hom.: 3928

Bravo AF: 0.561

Asia WGS AF: 0.744 AC: 2589 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
Cadd	Benign	3.8
Dann	Benign	0.49

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs9866825; hg19: chr3-8250790;