rs2622877

Positions:

• chr1-103004057-T-A
• chr1-103004057-T-C

Variant summary

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

The NM_001854.4(COL11A1):​c.1944+387A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.07 in 152,228 control chromosomes in the GnomAD database, including 455 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 0.070 (455 hom., cov: 32)
• Consequence: COL11A1 NM_001854.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.121

Genes affected

COL11A1 (HGNC:2186): (collagen type XI alpha 1 chain) This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Mutations in this gene are associated with type II Stickler syndrome and with Marshall syndrome. A single-nucleotide polymorphism in this gene is also associated with susceptibility to lumbar disc herniation. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]

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 (AFR) allele frequency at 95% confidence interval = 0.115 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
COL11A1	NM_001854.4	c.1944+387A>T		intron_variant		ENST00000370096.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
COL11A1	ENST00000370096.9	c.1944+387A>T		intron_variant		1	NM_001854.4	P1

Frequencies

GnomAD3 genomes AF: 0.0698 AC: 10618 AN: 152110 Hom.: 451 Cov.: 32

Gnomad AFR AF: 0.117

Gnomad AMI AF: 0.00439

Gnomad AMR AF: 0.0599

Gnomad ASJ AF: 0.0677

Gnomad EAS AF: 0.0719

Gnomad SAS AF: 0.0718

Gnomad FIN AF: 0.0497

Gnomad MID AF: 0.180

Gnomad NFE AF: 0.0465

Gnomad OTH AF: 0.0779

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.0700 AC: 10651 AN: 152228 Hom.: 455 Cov.: 32 AF XY: 0.0706 AC XY: 5255 AN XY: 74438

Gnomad4 AFR AF: 0.117

Gnomad4 AMR AF: 0.0598

Gnomad4 ASJ AF: 0.0677

Gnomad4 EAS AF: 0.0721

Gnomad4 SAS AF: 0.0720

Gnomad4 FIN AF: 0.0497

Gnomad4 NFE AF: 0.0465

Gnomad4 OTH AF: 0.0771

Alfa AF: 0.0143 Hom.: 4

Bravo AF: 0.0743

Asia WGS AF: 0.0730 AC: 251 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	4.3
DANN	Benign	0.38

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: rs2622877; hg19: chr1-103469613;