chr14-58467887-T-G

Variant names:

Variant summary

Our verdict is Uncertain significance. The variant received 3 ACMG points: 3P and 0B. PM2PP5

The NM_001329943.3(KIAA0586):c.2407T>G(p.Ser803Ala) variant causes a missense change. The variant allele was found at a frequency of 0.00000434 in 1,612,042 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Likely pathogenic (no stars).

Frequency

Genomes: 𝑓 0.0000066 ( 0 hom., cov: 32)

Exomes 𝑓: 0.0000041 ( 0 hom. )

Consequence

KIAA0586
NM_001329943.3 missense

Scores

Clinical Significance

Likely pathogenic no assertion criteria provided P:1

Conservation

PhyloP100: 5.43

Publications

2 publications found

Variant links:

Genes affected

KIAA0586 (HGNC:19960): (KIAA0586) This gene encodes a conserved centrosomal protein that functions in ciliogenesis and responds to hedgehog signaling. Mutations in this gene causes Joubert syndrome 23. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Aug 2016]

KIAA0586 Gene-Disease associations (from GenCC):

Joubert syndrome 23
Inheritance: AR Classification: DEFINITIVE, STRONG Submitted by: Labcorp Genetics (formerly Invitae), Ambry Genetics, G2P
short-rib thoracic dysplasia 14 with polydactyly
Inheritance: AR Classification: STRONG, MODERATE Submitted by: Ambry Genetics, Genomics England PanelApp, Labcorp Genetics (formerly Invitae)
Joubert syndrome
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
Joubert syndrome with Jeune asphyxiating thoracic dystrophy
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

KIAA0586 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Uncertain_significance. The variant received 3 ACMG points.

PM2

Very rare variant in population databases, with high coverage;

PP5

Variant 14-58467887-T-G is Pathogenic according to our data. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr14-58467887-T-G is described in CliVar as Likely_pathogenic. Clinvar id is 266094.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KIAA0586	NM_001329943.3 link	c.2407T>G	p.Ser803Ala	missense_variant	Exon 16 of 31	ENST00000652326.2	NP_001316872.1	A0A494C171

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KIAA0586	ENST00000652326.2 link	c.2407T>G	p.Ser803Ala	missense_variant	Exon 16 of 31		NM_001329943.3	ENSP00000498929.1		A0A494C171

Frequencies

GnomAD3 genomes

AF:

0.00000658

AC:

AN:

151904

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00

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:

0.0000147

Gnomad OTH

AF:

0.00

GnomAD4 exome

AF:

0.00000411

AC:

AN:

1460138

Hom.:

Cov.:

AF XY:

0.00000275

AC XY:

AN XY:

726392

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

33292

American (AMR)

AF:

0.00

AC:

AN:

44316

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26070

East Asian (EAS)

AF:

0.00

AC:

AN:

39670

South Asian (SAS)

AF:

0.00

AC:

AN:

86020

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53386

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5752

European-Non Finnish (NFE)

AF:

0.00000450

AC:

AN:

1111356

Other (OTH)

AF:

0.0000166

AC:

AN:

60276

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.450

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:

0.00000658

AC:

AN:

151904

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

74180

show subpopulations

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5.

African (AFR)

AF:

0.00

AC:

AN:

41340

American (AMR)

AF:

0.00

AC:

AN:

15254

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3468

East Asian (EAS)

AF:

0.00

AC:

AN:

5178

South Asian (SAS)

AF:

0.00

AC:

AN:

4812

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10570

Middle Eastern (MID)

AF:

0.00

AC:

AN:

316

European-Non Finnish (NFE)

AF:

0.0000147

AC:

AN:

67964

Other (OTH)

AF:

0.00

AC:

AN:

2090

⚠️ The allele balance in gnomAD version 4 Genomes is significantly skewed from the expected value of 0.5. (p-value = 0.000000), which strongly suggests a high chance of mosaicism in these individuals.

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.375

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:

0.00

Hom.:

ClinVar

Significance: Likely pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

LINK: link

Submissions by phenotype

Meckel-Gruber syndrome

Pathogenic:1

Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

Significance:Likely pathogenic

Review Status:no assertion criteria provided

Collection Method:research

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.19

BayesDel_addAF

Uncertain

0.014

BayesDel_noAF

Benign

-0.22

CADD

Uncertain

(source)

DANN

Uncertain

1.0

DEOGEN2

Benign

0.11

.;.;T;T;.;.

Eigen

Pathogenic

0.72

Eigen_PC

Pathogenic

0.70

FATHMM_MKL

Uncertain

0.90

LIST_S2

Benign

0.73

T;T;T;T;.;T

M_CAP

Benign

0.042

MetaRNN

Uncertain

0.47

T;T;T;T;T;T

MetaSVM

Uncertain

-0.24

MutationAssessor

Uncertain

2.4

.;.;.;M;.;.

PhyloP100

5.4

PrimateAI

Benign

0.48

PROVEAN

Benign

-1.9

N;.;.;.;N;N

REVEL

Benign

0.17

Sift

Benign

0.046

D;.;.;.;T;D

Sift4G

Benign

0.080

T;T;T;T;T;T

Polyphen

1.0

.;.;.;D;.;.

Vest4

0.53

MutPred

0.18

.;.;.;Gain of catalytic residue at P793 (P = 0);.;.;

MVP

0.81

MPC

0.15

ClinPred

0.94

GERP RS

5.6

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.7

Varity_R

0.23

gMVP

0.20

Mutation Taster

=2/98

disease causing (ClinVar)

(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

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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