21-45492744-G-GCCCGCCATTGCCCT

Variant names:

• chr21-45492744-G-GCCCGCCATTGCCCT
• NM_001379500.1:c.2214+35_2214+36insCCATTGCCCTCCCG

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 0P and 0B.

The NM_001379500.1(COL18A1):​c.2214+35_2214+36insCCATTGCCCTCCCG variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000715 in 1,399,390 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 0)
  • Exomes 𝑓: 0.0000071 (0 hom.)
• Consequence: COL18A1 NM_001379500.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.588

Genes affected

COL18A1 (HGNC:2195): (collagen type XVIII alpha 1 chain) This gene encodes the alpha chain of type XVIII collagen. This collagen is one of the multiplexins, extracellular matrix proteins that contain multiple triple-helix domains (collagenous domains) interrupted by non-collagenous domains. A long isoform of the protein has an N-terminal domain that is homologous to the extracellular part of frizzled receptors. Proteolytic processing at several endogenous cleavage sites in the C-terminal domain results in production of endostatin, a potent antiangiogenic protein that is able to inhibit angiogenesis and tumor growth. Mutations in this gene are associated with Knobloch syndrome. The main features of this syndrome involve retinal abnormalities, so type XVIII collagen may play an important role in retinal structure and in neural tube closure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
COL18A1	NM_001379500.1	c.2214+35_2214+36insCCATTGCCCTCCCG		intron_variant	Intron 24 of 41	ENST00000651438.1	NP_001366429.1
COL18A1	NM_130444.3	c.3459+35_3459+36insCCATTGCCCTCCCG		intron_variant	Intron 23 of 40		NP_569711.2
COL18A1	NM_030582.4	c.2754+35_2754+36insCCATTGCCCTCCCG		intron_variant	Intron 23 of 40		NP_085059.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
COL18A1	ENST00000651438.1	c.2214+31_2214+32insCCCGCCATTGCCCT		intron_variant	Intron 24 of 41		NM_001379500.1	ENSP00000498485.1
COL18A1	ENST00000355480.10	c.2754+31_2754+32insCCCGCCATTGCCCT		intron_variant	Intron 23 of 40	1		ENSP00000347665.5
COL18A1	ENST00000359759.8	c.3459+31_3459+32insCCCGCCATTGCCCT		intron_variant	Intron 23 of 40	5		ENSP00000352798.4
COL18A1	ENST00000342220.9	c.255+31_255+32insCCCGCCATTGCCCT		intron_variant	Intron 5 of 22	2		ENSP00000339118.5

Frequencies

GnomAD3 genomes Cov.: 0

GnomAD4 exome AF: 0.00000715 AC: 10 AN: 1399390 Hom.: 0 Cov.: 28 AF XY: 0.00000429 AC XY: 3 AN XY: 699236

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.00000939

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr21-46912658;