8-1771069-C-T

Variant names:

Variant summary

Our verdict is Benign. The variant received -13 ACMG points: 0P and 13B. BP4_StrongBP6_Very_StrongBP7

The NM_018941.4(CLN8):c.15C>T(p.Ser5Ser) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000663 in 1,613,836 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.000072 ( 0 hom., cov: 32)

Exomes 𝑓: 0.000066 ( 0 hom. )

Consequence

CLN8
NM_018941.4 synonymous

Scores

Clinical Significance

Likely benign criteria provided, multiple submitters, no conflicts B:2

Conservation

PhyloP100: -0.911

Publications

0 publications found

Variant links:

Genes affected

CLN8 (HGNC:2079): (CLN8 transmembrane ER and ERGIC protein) This gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER-Golgi intermediate compartment. Mutations in this gene are associated with a disorder characterized by progressive epilepsy with cognitive disabilities (EPMR), which is a subtype of neuronal ceroid lipofuscinoses (NCL). Patients with mutations in this gene have altered levels of sphingolipid and phospholipids in the brain. [provided by RefSeq, Jul 2017]

CLN8 Gene-Disease associations (from GenCC):

neuronal ceroid lipofuscinosis
Inheritance: AR Classification: DEFINITIVE Submitted by: ClinGen
neuronal ceroid lipofuscinosis 8
Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), Genomics England PanelApp, G2P, Orphanet, Ambry Genetics, Myriad Women’s Health
neuronal ceroid lipofuscinosis 8 northern epilepsy variant
Inheritance: AR Classification: STRONG, SUPPORTIVE Submitted by: Genomics England PanelApp, Orphanet
autism spectrum disorder
Inheritance: AD Classification: NO_KNOWN Submitted by: Ambry Genetics

CLN8 links:

KBTBD11-OT1 (HGNC:):

KBTBD11-OT1 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -13 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.76).

BP6

Variant 8-1771069-C-T is Benign according to our data. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr8-1771069-C-T is described in CliVar as Likely_benign. Clinvar id is 377698.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=-0.911 with no splicing effect.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CLN8	NM_018941.4 link	c.15C>T	p.Ser5Ser	synonymous_variant	Exon 2 of 3	ENST00000331222.6	NP_061764.2	Q9UBY8A0A024QZ57

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CLN8	ENST00000331222.6 link	c.15C>T	p.Ser5Ser	synonymous_variant	Exon 2 of 3	1	NM_018941.4	ENSP00000328182.4		Q9UBY8
KBTBD11-OT1	ENST00000635855.1 link	n.15C>T		non_coding_transcript_exon_variant	Exon 2 of 30	5		ENSP00000489726.1		A0A1B0GTJ5

Frequencies

GnomAD3 genomes

AF:

0.0000724

AC:

AN:

152002

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00

Gnomad AMI

AF:

0.00439

Gnomad AMR

AF:

0.0000655

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.0000882

Gnomad OTH

AF:

0.00

GnomAD2 exomes

AF:

0.0000477

AC:

AN:

251476

AF XY:

0.0000294

show subpopulations

Gnomad AFR exome

AF:

0.00

Gnomad AMR exome

AF:

0.0000578

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.0000879

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.0000657

AC:

AN:

1461834

Hom.:

Cov.:

AF XY:

0.0000564

AC XY:

AN XY:

727214

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

33480

American (AMR)

AF:

0.0000894

AC:

AN:

44724

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26136

East Asian (EAS)

AF:

0.00

AC:

AN:

39700

South Asian (SAS)

AF:

0.00

AC:

AN:

86258

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53382

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5768

European-Non Finnish (NFE)

AF:

0.0000791

AC:

AN:

1111990

Other (OTH)

AF:

0.0000662

AC:

AN:

60396

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.446

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

<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:

0.0000724

AC:

AN:

152002

Hom.:

Cov.:

AF XY:

0.0000674

AC XY:

AN XY:

74222

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

41398

American (AMR)

AF:

0.0000655

AC:

AN:

15260

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3470

East Asian (EAS)

AF:

0.00

AC:

AN:

5148

South Asian (SAS)

AF:

0.00

AC:

AN:

4820

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10576

Middle Eastern (MID)

AF:

0.00

AC:

AN:

316

European-Non Finnish (NFE)

AF:

0.0000882

AC:

AN:

68014

Other (OTH)

AF:

0.00

AC:

AN:

2088

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.470

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Variant carriers

<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:

0.0000823

Hom.:

Bravo

AF:

0.0000793

EpiCase

AF:

0.00

EpiControl

AF:

0.000119

ClinVar

Significance: Likely benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:1

Jun 03, 2019

GeneDx

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Neuronal ceroid lipofuscinosis

Benign:1

Nov 05, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.76

CADD

Benign

0.67

(source)

DANN

Benign

0.63

PhyloP100

-0.91

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.7

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over