rs72857800

Variant names:

• chr1-11934559-G-A
• rs72857800
• ENST00000485046.5:n.119+236G>A

Your query was ambiguous. Multiple possible variants found:

• chr1-11934559-G-A
• chr1-11934559-G-C
• chr1-11934559-G-T

Variant summary

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

The ENST00000485046.5(PLOD1):​n.119+236G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000235 in 425,846 control chromosomes in the GnomAD database, with no homozygous occurrence. 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)
  • Exomes 𝑓: 0.0000023 (0 hom.)
• Consequence: PLOD1 ENST00000485046.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.34
• Publications: 0 publications found

Genes affected

PLOD1 (HGNC:9081): (procollagen-lysine,2-oxoglutarate 5-dioxygenase 1) Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]

PLOD1 Gene-Disease associations (from GenCC):

• Ehlers-Danlos syndrome, kyphoscoliotic type 1

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), Genomics England PanelApp, Orphanet, PanelApp Australia, G2P

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=-0.78).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PLOD1	NM_000302.4	c.-221G>A		upstream_gene_variant		ENST00000196061.5	NP_000293.2
PLOD1	NM_001316320.2	c.-221G>A		upstream_gene_variant			NP_001303249.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PLOD1	ENST00000196061.5	c.-221G>A		upstream_gene_variant		1	NM_000302.4	ENSP00000196061.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome AF: 0.00000235 AC: 1 AN: 425846 Hom.: 0 AF XY: 0.00000453 AC XY: 1 AN XY: 220608

African (AFR) AF: 0.00 AC: 0 AN: 8454

American (AMR) AF: 0.00 AC: 0 AN: 7196

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 10796

East Asian (EAS) AF: 0.0000456 AC: 1 AN: 21924

South Asian (SAS) AF: 0.00 AC: 0 AN: 33172

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 26688

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 1738

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 292842

Other (OTH) AF: 0.00 AC: 0 AN: 23036

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	3.0
DANN	Benign	0.92
PhyloP100		-1.3
PromoterAI		-0.011	Neutral

Splicing

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

Other links and lift over

dbSNP: rs72857800; hg19: chr1-11994616;