NM_001849.4:c.2724A>G

Variant names:

Variant summary

Our verdict is Benign. The variant received -21 ACMG points: 0P and 21B. BP4_StrongBP6_Very_StrongBP7BA1

The NM_001849.4(COL6A2):c.2724A>G(p.Thr908Thr) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.107 in 1,592,298 control chromosomes in the GnomAD database, including 10,849 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.14 ( 1871 hom., cov: 34)

Exomes 𝑓: 0.10 ( 8978 hom. )

Consequence

COL6A2
NM_001849.4 synonymous

Scores

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:13

Conservation

PhyloP100: -0.0370

Publications

8 publications found

Variant links:

Genes affected

COL6A2 (HGNC:2212): (collagen type VI alpha 2 chain) This gene encodes one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The product of this gene contains several domains similar to von Willebrand Factor type A domains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in this gene are associated with Bethlem myopathy and Ullrich scleroatonic muscular dystrophy. Three transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]

COL6A2 Gene-Disease associations (from GenCC):

collagen 6-related myopathy
Inheritance: AD, SD, AR Classification: DEFINITIVE Submitted by: ClinGen
Ullrich congenital muscular dystrophy 1B
Inheritance: AR, AD Classification: DEFINITIVE Submitted by: G2P
Bethlem myopathy 1A
Inheritance: AD, AR Classification: STRONG Submitted by: Genomics England PanelApp
Ullrich congenital muscular dystrophy 1A
Inheritance: AR, AD Classification: STRONG Submitted by: Genomics England PanelApp, Labcorp Genetics (formerly Invitae)
Bethlem myopathy
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
Ullrich congenital muscular dystrophy
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
myosclerosis
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

COL6A2 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -21 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.93).

BP6

Variant 21-46132216-A-G is Benign according to our data. Variant chr21-46132216-A-G is described in ClinVar as Benign. ClinVar VariationId is 93945.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=-0.037 with no splicing effect.

BA1

GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.254 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001849.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	COL6A2	NM_001849.4	MANE Select	c.2724A>G	p.Thr908Thr	synonymous	Exon 28 of 28	NP_001840.3

Ensembl Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
COL6A2	ENST00000300527.9	TSL:1 MANE Select	c.2724A>G	p.Thr908Thr	synonymous	Exon 28 of 28	ENSP00000300527.4	P12110-1
COL6A2	ENST00000857098.1		c.2919A>G	p.Thr973Thr	synonymous	Exon 28 of 28	ENSP00000527157.1
COL6A2	ENST00000857103.1		c.2886A>G	p.Thr962Thr	synonymous	Exon 28 of 28	ENSP00000527162.1

Frequencies

GnomAD3 genomes

AF:

0.137

AC:

20795

AN:

152062

Hom.:

1868

Cov.:

show subpopulations

Gnomad AFR

AF:

0.258

Gnomad AMI

AF:

0.0714

Gnomad AMR

AF:

0.0802

Gnomad ASJ

AF:

0.0882

Gnomad EAS

AF:

0.0254

Gnomad SAS

AF:

0.182

Gnomad FIN

AF:

0.0371

Gnomad MID

AF:

0.133

Gnomad NFE

AF:

0.100

Gnomad OTH

AF:

0.128

GnomAD2 exomes

AF:

0.0984

AC:

20809

AN:

211458

AF XY:

0.102

show subpopulations

Gnomad AFR exome

AF:

0.259

Gnomad AMR exome

AF:

0.0521

Gnomad ASJ exome

AF:

0.0871

Gnomad EAS exome

AF:

0.0247

Gnomad FIN exome

AF:

0.0329

Gnomad NFE exome

AF:

0.0960

Gnomad OTH exome

AF:

0.0888

GnomAD4 exome

AF:

0.104

AC:

149607

AN:

1440118

Hom.:

8978

Cov.:

AF XY:

0.105

AC XY:

75356

AN XY:

715164

show subpopulations

African (AFR)

AF:

0.265

AC:

8722

AN:

32886

American (AMR)

AF:

0.0560

AC:

2351

AN:

41960

Ashkenazi Jewish (ASJ)

AF:

0.0901

AC:

2318

AN:

25736

East Asian (EAS)

AF:

0.0220

AC:

843

AN:

38300

South Asian (SAS)

AF:

0.169

AC:

14205

AN:

83856

European-Finnish (FIN)

AF:

0.0389

AC:

1921

AN:

49386

Middle Eastern (MID)

AF:

0.127

AC:

727

AN:

5744

European-Non Finnish (NFE)

AF:

0.102

AC:

112022

AN:

1102638

Other (OTH)

AF:

0.109

AC:

6498

AN:

59612

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.474

Heterozygous variant carriers

10233

20466

30700

40933

51166

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

Variant carriers

4208

8416

12624

16832

21040

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.137

AC:

20844

AN:

152180

Hom.:

1871

Cov.:

AF XY:

0.133

AC XY:

9881

AN XY:

74414

show subpopulations

African (AFR)

AF:

0.258

AC:

10726

AN:

41494

American (AMR)

AF:

0.0800

AC:

1223

AN:

15290

Ashkenazi Jewish (ASJ)

AF:

0.0882

AC:

306

AN:

3470

East Asian (EAS)

AF:

0.0255

AC:

132

AN:

5176

South Asian (SAS)

AF:

0.182

AC:

877

AN:

4824

European-Finnish (FIN)

AF:

0.0371

AC:

394

AN:

10612

Middle Eastern (MID)

AF:

0.122

AC:

AN:

294

European-Non Finnish (NFE)

AF:

0.100

AC:

6806

AN:

67996

Other (OTH)

AF:

0.132

AC:

279

AN:

2114

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.502

Heterozygous variant carriers

893

1786

2679

3572

4465

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

234

468

702

936

1170

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.109

Hom.:

383

Bravo

AF:

0.144

Asia WGS

AF:

0.144

AC:

504

AN:

3478

ClinVar

ClinVar submissions

Significance:Benign

Revision:criteria provided, multiple submitters, no conflicts

View on ClinVar

Pathogenic

VUS

Benign

Condition

not specified (6)

not provided (3)

Bethlem myopathy 1A (1)

Collagen 6-related myopathy (1)

Glutamate formiminotransferase deficiency (1)

Myosclerosis (1)

Computational scores

Source: dbNSFP v4.9

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.93

CADD

Benign

0.27

(source)

DANN

Benign

0.28

PhyloP100

-0.037

Mutation Taster

=100/0

polymorphism (auto)

(source)

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

You must be logged in to view publications. This limit was set because tens of millions (!) of queries from AI bots are generated daily.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Variant Effect in Transcripts

RefSeq Transcripts

Ensembl Transcripts

Frequencies

Age Distribution

Age Distribution

ClinVar

Computational scores

Splicing

Publications

Other links and lift over