chr13-110206969-GA-G

Position:

• chr13-110206969-GA-G

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP6_Moderate BA1

The NM_001845.6(COL4A1):​c.781-79del variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.256 in 1,144,856 control chromosomes in the GnomAD database, including 14,618 homozygotes. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.27 (5032 hom., cov: 18)
  • Exomes 𝑓: 0.25 (9586 hom.)
• Consequence: COL4A1 NM_001845.6 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.896

Genes affected

COL4A1 (HGNC:2202): (collagen type IV alpha 1 chain) This gene encodes a type IV collagen alpha protein. Type IV collagen proteins are integral components of basement membranes. This gene shares a bidirectional promoter with a paralogous gene on the opposite strand. The protein consists of an amino-terminal 7S domain, a triple-helix forming collagenous domain, and a carboxy-terminal non-collagenous domain. It functions as part of a heterotrimer and interacts with other extracellular matrix components such as perlecans, proteoglycans, and laminins. In addition, proteolytic cleavage of the non-collagenous carboxy-terminal domain results in a biologically active fragment known as arresten, which has anti-angiogenic and tumor suppressor properties. Mutations in this gene cause porencephaly, cerebrovascular disease, and renal and muscular defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP6: Variant 13-110206969-GA-G is Benign according to our data. Variant chr13-110206969-GA-G is described in ClinVar as [Benign]. Clinvar id is 1250990.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.328 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
COL4A1	NM_001845.6	c.781-79del		intron_variant		ENST00000375820.10
COL4A1	NM_001303110.2	c.781-79del		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
COL4A1	ENST00000375820.10	c.781-79del		intron_variant		1	NM_001845.6	P1

Frequencies

GnomAD3 genomes AF: 0.272 AC: 38126 AN: 140118 Hom.: 5022 Cov.: 18

Gnomad AFR AF: 0.251

Gnomad AMI AF: 0.0696

Gnomad AMR AF: 0.335

Gnomad ASJ AF: 0.257

Gnomad EAS AF: 0.0519

Gnomad SAS AF: 0.225

Gnomad FIN AF: 0.362

Gnomad MID AF: 0.276

Gnomad NFE AF: 0.282

Gnomad OTH AF: 0.237

GnomAD4 exome AF: 0.254 AC: 254724 AN: 1004676 Hom.: 9586 AF XY: 0.253 AC XY: 129133 AN XY: 510168

Gnomad4 AFR exome AF: 0.233

Gnomad4 AMR exome AF: 0.322

Gnomad4 ASJ exome AF: 0.239

Gnomad4 EAS exome AF: 0.0480

Gnomad4 SAS exome AF: 0.228

Gnomad4 FIN exome AF: 0.309

Gnomad4 NFE exome AF: 0.260

Gnomad4 OTH exome AF: 0.246

GnomAD4 genome AF: 0.272 AC: 38172 AN: 140180 Hom.: 5032 Cov.: 18 AF XY: 0.276 AC XY: 18785 AN XY: 67978

Gnomad4 AFR AF: 0.252

Gnomad4 AMR AF: 0.336

Gnomad4 ASJ AF: 0.257

Gnomad4 EAS AF: 0.0517

Gnomad4 SAS AF: 0.226

Gnomad4 FIN AF: 0.362

Gnomad4 NFE AF: 0.282

Gnomad4 OTH AF: 0.235

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Aug 24, 2019

- -

Computational scores

Source: dbNSFP v4.3

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: rs60585275; hg19: chr13-110859316;