chr21-45512738-G-C

Variant names:

• chr21-45512738-G-C
• rs7867
• NM_001379500.1:c.*340G>C

Variant summary

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

The NM_001379500.1(COL18A1):​c.*340G>C variant causes a 3 prime UTR 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: 33)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: COL18A1 NM_001379500.1 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.473
• Publications: 13 publications found

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]

SLC19A1 (HGNC:10937): (solute carrier family 19 member 1) The membrane protein encoded by this gene is a transporter of folate and is involved in the regulation of intracellular concentrations of folate. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]

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=-0.85).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001379500.1. 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
	COL18A1	NM_001379500.1	MANE Select	c.*340G>C		3_prime_UTR	Exon 42 of 42	NP_001366429.1
	SLC19A1	NM_194255.4	MANE Select	c.*2920C>G		3_prime_UTR	Exon 6 of 6	NP_919231.1
	COL18A1	NM_130444.3		c.*340G>C		3_prime_UTR	Exon 41 of 41	NP_569711.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	COL18A1	ENST00000651438.1	MANE Select	c.*340G>C		3_prime_UTR	Exon 42 of 42	ENSP00000498485.1
	SLC19A1	ENST00000311124.9	TSL:1 MANE Select	c.*2920C>G		3_prime_UTR	Exon 6 of 6	ENSP00000308895.4
	COL18A1	ENST00000355480.10	TSL:1	c.*340G>C		3_prime_UTR	Exon 41 of 41	ENSP00000347665.5

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 244550 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 130200

African (AFR) AF: 0.00 AC: 0 AN: 7344

American (AMR) AF: 0.00 AC: 0 AN: 10122

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 6886

East Asian (EAS) AF: 0.00 AC: 0 AN: 12000

South Asian (SAS) AF: 0.00 AC: 0 AN: 38768

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 12158

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 976

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 143194

Other (OTH) AF: 0.00 AC: 0 AN: 13102

GnomAD4 genome Cov.: 33

Alfa AF: 0.00 Hom.: 34122

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	4.8
DANN	Benign	0.81
PhyloP100		-0.47

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: rs7867; hg19: chr21-46932652;