1-102976258-A-G

Position:

• chr1-102976258-A-G

Variant summary

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

The NM_001854.4(COL11A1):​c.2755-1375T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.416 in 141,718 control chromosomes in the GnomAD database, including 14,142 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 0.42 (14142 hom., cov: 25)
• Consequence: COL11A1 NM_001854.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0110

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=-0.96).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.782 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
COL11A1	NM_001854.4	c.2755-1375T>C		intron_variant		ENST00000370096.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
COL11A1	ENST00000370096.9	c.2755-1375T>C		intron_variant		1	NM_001854.4	P1

Frequencies

GnomAD3 genomes AF: 0.416 AC: 58871 AN: 141614 Hom.: 14134 Cov.: 25

Gnomad AFR AF: 0.157

Gnomad AMI AF: 0.569

Gnomad AMR AF: 0.534

Gnomad ASJ AF: 0.432

Gnomad EAS AF: 0.803

Gnomad SAS AF: 0.486

Gnomad FIN AF: 0.457

Gnomad MID AF: 0.444

Gnomad NFE AF: 0.504

Gnomad OTH AF: 0.449

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

GnomAD4 genome AF: 0.416 AC: 58889 AN: 141718 Hom.: 14142 Cov.: 25 AF XY: 0.416 AC XY: 28340 AN XY: 68066

Gnomad4 AFR AF: 0.156

Gnomad4 AMR AF: 0.534

Gnomad4 ASJ AF: 0.432

Gnomad4 EAS AF: 0.803

Gnomad4 SAS AF: 0.486

Gnomad4 FIN AF: 0.457

Gnomad4 NFE AF: 0.504

Gnomad4 OTH AF: 0.453

Alfa AF: 0.475 Hom.: 16080

Bravo AF: 0.415

Asia WGS AF: 0.599 AC: 2072 AN: 3464

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	0.58
DANN	Benign	0.40

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: rs2061705; hg19: chr1-103441814; COSMIC: COSV62177118;