chr6-33166615-C-A

Variant names:

• chr6-33166615-C-A
• rs2855453
• NM_080680.3:c.4339-49G>T

Variant summary

Our verdict is Benign. The variant received -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The ENST00000341947.7(COL11A2):​c.4339-49G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.688 in 1,611,724 control chromosomes in the GnomAD database, including 386,095 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.68 (35422 hom., cov: 29)
  • Exomes 𝑓: 0.69 (350673 hom.)
• Consequence: COL11A2 ENST00000341947.7 intron
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:6
• Conservation: PhyloP100: 0.753
• Publications: 16 publications found

Genes affected

COL11A2 (HGNC:2187): (collagen type XI alpha 2 chain) This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]

COL11A2 Gene-Disease associations (from GenCC):

• autosomal dominant nonsyndromic hearing loss 13

  Inheritance: AD Classification: DEFINITIVE, STRONG, MODERATE, LIMITED Submitted by: Ambry Genetics, PanelApp Australia, Labcorp Genetics (formerly Invitae), G2P
• nonsyndromic genetic hearing loss

  Inheritance: AD, AR Classification: DEFINITIVE, MODERATE Submitted by: ClinGen
• otospondylomegaepiphyseal dysplasia, autosomal dominant

  Inheritance: AD Classification: DEFINITIVE, STRONG, MODERATE, SUPPORTIVE Submitted by: PanelApp Australia, Ambry Genetics, Orphanet, Genomics England PanelApp, Labcorp Genetics (formerly Invitae), G2P
• autosomal recessive nonsyndromic hearing loss 53

  Inheritance: AR Classification: DEFINITIVE, STRONG, MODERATE Submitted by: G2P, PanelApp Australia, Ambry Genetics, Labcorp Genetics (formerly Invitae)
• otospondylomegaepiphyseal dysplasia

  Inheritance: AR, AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: Orphanet, ClinGen
• otospondylomegaepiphyseal dysplasia, autosomal recessive

  Inheritance: AR Classification: DEFINITIVE, STRONG, MODERATE Submitted by: PanelApp Australia, Ambry Genetics, G2P, Labcorp Genetics (formerly Invitae)
• autosomal dominant nonsyndromic hearing loss

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• fibrochondrogenesis

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• hearing loss, autosomal recessive

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Benign. The variant received -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BP6: Variant 6-33166615-C-A is Benign according to our data. Variant chr6-33166615-C-A is described in ClinVar as Benign. ClinVar VariationId is 674799.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.942 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000341947.7. 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
	COL11A2	NM_080680.3	MANE Select	c.4339-49G>T		intron	N/A	NP_542411.2
	COL11A2	NM_001424108.1		c.4159-49G>T		intron	N/A	NP_001411037.1
	COL11A2	NM_080681.3		c.4081-49G>T		intron	N/A	NP_542412.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	COL11A2	ENST00000341947.7	TSL:5 MANE Select	c.4339-49G>T		intron	N/A	ENSP00000339915.2
	COL11A2	ENST00000374708.8	TSL:5	c.4081-49G>T		intron	N/A	ENSP00000363840.4
	COL11A2	ENST00000477772.1	TSL:2	n.273-799G>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.679 AC: 102845 AN: 151548 Hom.: 35392 Cov.: 29

Gnomad AFR AF: 0.607

Gnomad AMI AF: 0.597

Gnomad AMR AF: 0.742

Gnomad ASJ AF: 0.824

Gnomad EAS AF: 0.964

Gnomad SAS AF: 0.840

Gnomad FIN AF: 0.660

Gnomad MID AF: 0.812

Gnomad NFE AF: 0.669

Gnomad OTH AF: 0.713

GnomAD2 exomes AF: 0.732 AC: 180080 AN: 246104 AF XY: 0.736

Gnomad AFR exome AF: 0.603

Gnomad AMR exome AF: 0.781

Gnomad ASJ exome AF: 0.834

Gnomad EAS exome AF: 0.970

Gnomad FIN exome AF: 0.648

Gnomad NFE exome AF: 0.675

Gnomad OTH exome AF: 0.749

GnomAD4 exome AF: 0.689 AC: 1005966 AN: 1460058 Hom.: 350673 Cov.: 40 AF XY: 0.694 AC XY: 504122 AN XY: 726344

African (AFR) AF: 0.590 AC: 19728 AN: 33430

American (AMR) AF: 0.780 AC: 34735 AN: 44534

Ashkenazi Jewish (ASJ) AF: 0.833 AC: 21741 AN: 26108

East Asian (EAS) AF: 0.980 AC: 38889 AN: 39680

South Asian (SAS) AF: 0.825 AC: 71133 AN: 86204

European-Finnish (FIN) AF: 0.651 AC: 34653 AN: 53230

Middle Eastern (MID) AF: 0.815 AC: 4699 AN: 5764

European-Non Finnish (NFE) AF: 0.664 AC: 737424 AN: 1110778

Other (OTH) AF: 0.712 AC: 42964 AN: 60330

GnomAD4 genome AF: 0.679 AC: 102931 AN: 151666 Hom.: 35422 Cov.: 29 AF XY: 0.684 AC XY: 50668 AN XY: 74116

African (AFR) AF: 0.607 AC: 25081 AN: 41292

American (AMR) AF: 0.742 AC: 11331 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.824 AC: 2861 AN: 3470

East Asian (EAS) AF: 0.964 AC: 4945 AN: 5130

South Asian (SAS) AF: 0.841 AC: 4038 AN: 4804

European-Finnish (FIN) AF: 0.660 AC: 6951 AN: 10530

Middle Eastern (MID) AF: 0.818 AC: 239 AN: 292

European-Non Finnish (NFE) AF: 0.669 AC: 45444 AN: 67878

Other (OTH) AF: 0.716 AC: 1501 AN: 2096

Alfa AF: 0.691 Hom.: 53109

Bravo AF: 0.684

Asia WGS AF: 0.859 AC: 2987 AN: 3478

ClinVar

ClinVar submissions as Germline

Significance: Benign

Revision: criteria provided, multiple submitters, no conflicts

Pathogenic	VUS	Benign	Condition
-	-	1	Autosomal dominant nonsyndromic hearing loss 13 (1)
-	-	1	Autosomal recessive nonsyndromic hearing loss 53 (1)
-	-	1	Fibrochondrogenesis 2 (1)
-	-	1	not provided (1)
-	-	1	Otospondylomegaepiphyseal dysplasia, autosomal dominant (1)
-	-	1	Otospondylomegaepiphyseal dysplasia, autosomal recessive (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	4.7
DANN	Benign	0.74
PhyloP100		0.75
Mutation Taster		=100/0	polymorphism (auto)

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: rs2855453; hg19: chr6-33134392; COSMIC: COSV59503025;