chr10-69954168-T-C

Position:

• chr10-69954168-T-C

Variant summary

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

The NM_001368882.1(COL13A1):​c.2145+1200T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.392 in 152,490 control chromosomes in the GnomAD database, including 12,283 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 0.39 (12270 hom., cov: 32)
  • Exomes 𝑓: 0.24 (13 hom.)
• Consequence: COL13A1 NM_001368882.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0650

Genes affected

COL13A1 (HGNC:2190): (collagen type XIII alpha 1 chain) This gene encodes the alpha chain of one of the nonfibrillar collagens. The function of this gene product is not known, however, it has been detected at low levels in all connective tissue-producing cells so it may serve a general function in connective tissues. Unlike most of the collagens, which are secreted into the extracellular matrix, collagen XIII contains a transmembrane domain and the protein has been localized to the plasma membrane. The transcripts for this gene undergo complex and extensive splicing involving at least eight exons. Like other collagens, collagen XIII is a trimer; it is not known whether this trimer is composed of one or more than one alpha chain isomer. A number of alternatively spliced transcript variants have been described, but the full length nature of some of them has not been determined. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.507 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
COL13A1	NM_001368882.1	c.2145+1200T>C		intron_variant		ENST00000645393.2	NP_001355811.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
COL13A1	ENST00000645393.2	c.2145+1200T>C		intron_variant			NM_001368882.1	ENSP00000496051	P1

Frequencies

GnomAD3 genomes AF: 0.393 AC: 59619 AN: 151878 Hom.: 12231 Cov.: 32

Gnomad AFR AF: 0.498

Gnomad AMI AF: 0.345

Gnomad AMR AF: 0.398

Gnomad ASJ AF: 0.363

Gnomad EAS AF: 0.524

Gnomad SAS AF: 0.408

Gnomad FIN AF: 0.261

Gnomad MID AF: 0.389

Gnomad NFE AF: 0.338

Gnomad OTH AF: 0.417

GnomAD4 exome AF: 0.245 AC: 121 AN: 494 Hom.: 13 AF XY: 0.213 AC XY: 66 AN XY: 310

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.167

Gnomad4 SAS exome AF: 0.750

Gnomad4 FIN exome AF: 0.230

Gnomad4 NFE exome AF: 0.333

Gnomad4 OTH exome AF: 0.188

GnomAD4 genome AF: 0.393 AC: 59705 AN: 151996 Hom.: 12270 Cov.: 32 AF XY: 0.392 AC XY: 29128 AN XY: 74290

Gnomad4 AFR AF: 0.498

Gnomad4 AMR AF: 0.398

Gnomad4 ASJ AF: 0.363

Gnomad4 EAS AF: 0.523

Gnomad4 SAS AF: 0.407

Gnomad4 FIN AF: 0.261

Gnomad4 NFE AF: 0.338

Gnomad4 OTH AF: 0.421

Alfa AF: 0.355 Hom.: 12776

Bravo AF: 0.409

Asia WGS AF: 0.462 AC: 1602 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	3.3
DANN	Benign	0.43

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

Publications

LitVar

Other links and lift over

dbSNP: rs2394615; hg19: chr10-71713924;