rs829584

Variant names:

• chr2-30454409-A-C
• rs829584
• NM_001002257.3:c.-5+7026A>C

Your query was ambiguous. Multiple possible variants found:

• chr2-30454409-A-C
• chr2-30454409-A-G

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The ENST00000379509.8(LCLAT1):​c.-5+7026A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 32)
• Consequence: LCLAT1 ENST00000379509.8 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.674
• Publications: 17 publications found

Genes affected

LCLAT1 (HGNC:26756): (lysocardiolipin acyltransferase 1) Enables 1-acylglycerol-3-phosphate O-acyltransferase activity. Predicted to be involved in phosphatidylinositol acyl-chain remodeling. Located in cytosol and endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000379509.8. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LCLAT1	NM_001002257.3	MANE Select	c.-5+7026A>C		intron	N/A	NP_001002257.1
	LCLAT1	NM_182551.5		c.-61-5143A>C		intron	N/A	NP_872357.2
	LCLAT1	NM_001304445.2		c.-409-5143A>C		intron	N/A	NP_001291374.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LCLAT1	ENST00000379509.8	TSL:1 MANE Select	c.-5+7026A>C		intron	N/A	ENSP00000368823.3
	LCLAT1	ENST00000309052.8	TSL:1	c.-61-5143A>C		intron	N/A	ENSP00000310551.4
	LCLAT1	ENST00000319406.8	TSL:2	c.-61-5143A>C		intron	N/A	ENSP00000368826.1

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	7.3
DANN	Benign	0.90
PhyloP100		0.67

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Other links and lift over

dbSNP: rs829584; hg19: chr2-30677275;