X-111410060-G-T

Variant names:

Variant summary

Our verdict is Benign. The variant received -17 ACMG points: 0P and 17B. BP4_StrongBP6_Very_StrongBP7BS2

The NM_001195553.2(DCX):c.339C>A(p.Ile113Ile) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0000422 in 1,209,711 control chromosomes in the GnomAD database, including 1 homozygotes. There are 21 hemizygotes in GnomAD. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.0000090 ( 0 hom., 0 hem., cov: 22)

Exomes 𝑓: 0.000046 ( 1 hom. 21 hem. )

Consequence

DCX
NM_001195553.2 synonymous

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:3

Conservation

PhyloP100: -0.207

Publications

0 publications found

Variant links:

Genes affected

DCX (HGNC:2714): (doublecortin) This gene encodes a member of the doublecortin family. The protein encoded by this gene is a cytoplasmic protein and contains two doublecortin domains, which bind microtubules. In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The encoded protein appears to direct neuronal migration by regulating the organization and stability of microtubules. In addition, the encoded protein interacts with LIS1, the regulatory gamma subunit of platelet activating factor acetylhydrolase, and this interaction is important to proper microtubule function in the developing cortex. Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex, leading to epilepsy, cognitive disability, subcortical band heterotopia ("double cortex" syndrome) in females and lissencephaly ("smooth brain" syndrome) in males. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]

DCX Gene-Disease associations (from GenCC):

lissencephaly spectrum disorders
Inheritance: XL Classification: DEFINITIVE Submitted by: ClinGen
lissencephaly type 1 due to doublecortin gene mutation
Inheritance: XL Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, Labcorp Genetics (formerly Invitae), G2P
subcortical band heterotopia
Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

DCX links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -17 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.52).

BP6

Variant X-111410060-G-T is Benign according to our data. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chrX-111410060-G-T is described in CliVar as Benign/Likely_benign. Clinvar id is 158455.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=-0.207 with no splicing effect.

BS2

High Hemizygotes in GnomAdExome4 at 21 XL,AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DCX	NM_001195553.2 link	c.339C>A	p.Ile113Ile	synonymous_variant	Exon 2 of 7	ENST00000636035.2	NP_001182482.1	A8K340

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	UniProt
DCX	ENST00000636035.2 link	c.339C>A	p.Ile113Ile	synonymous_variant	Exon 2 of 7	2	NM_001195553.2	ENSP00000490614.1	A8K340
DCX	ENST00000356220.8 link	c.339C>A	p.Ile113Ile	synonymous_variant	Exon 3 of 8	5		ENSP00000348553.4	A8K340
DCX	ENST00000637453.1 link	c.339C>A	p.Ile113Ile	synonymous_variant	Exon 2 of 7	5		ENSP00000490357.1	A8K340
DCX	ENST00000637570.1 link	c.339C>A	p.Ile113Ile	synonymous_variant	Exon 2 of 7	5		ENSP00000490878.1	A0A1B0GWD1

Frequencies

GnomAD3 genomes

AF:

0.00000896

AC:

AN:

111616

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:

0.0000188

Gnomad OTH

AF:

0.00

GnomAD2 exomes

AF:

0.0000601

AC:

AN:

183039

AF XY:

0.0000443

show subpopulations

Gnomad AFR exome

AF:

0.00

Gnomad AMR exome

AF:

0.00

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.000123

Gnomad OTH exome

AF:

0.000221

GnomAD4 exome

AF:

0.0000455

AC:

AN:

1098095

Hom.:

Cov.:

AF XY:

0.0000578

AC XY:

AN XY:

363503

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

26400

American (AMR)

AF:

0.00

AC:

AN:

35207

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

19384

East Asian (EAS)

AF:

0.00

AC:

AN:

30181

South Asian (SAS)

AF:

0.00

AC:

AN:

54139

European-Finnish (FIN)

AF:

0.00

AC:

AN:

40528

Middle Eastern (MID)

AF:

0.00

AC:

AN:

4130

European-Non Finnish (NFE)

AF:

0.0000487

AC:

AN:

842033

Other (OTH)

AF:

0.000195

AC:

AN:

46093

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.475

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

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:

0.00000896

AC:

AN:

111616

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

33810

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

30651

American (AMR)

AF:

0.00

AC:

AN:

10516

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

2643

East Asian (EAS)

AF:

0.00

AC:

AN:

3568

South Asian (SAS)

AF:

0.00

AC:

AN:

2618

European-Finnish (FIN)

AF:

0.00

AC:

AN:

6048

Middle Eastern (MID)

AF:

0.00

AC:

AN:

239

European-Non Finnish (NFE)

AF:

0.0000188

AC:

AN:

53146

Other (OTH)

AF:

0.00

AC:

AN:

1501

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.475

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Alfa

AF:

0.00

Hom.:

Bravo

AF:

0.0000264

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:3

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:2

Dec 01, 2020

CeGaT Center for Human Genetics Tuebingen

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Apr 17, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

not specified

Benign:1

Feb 08, 2013

Genetic Services Laboratory, University of Chicago

Significance: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

-0.52

CADD

Benign

1.8

(source)

DANN

Benign

0.71

PhyloP100

-0.21

PromoterAI

-0.11

Neutral

(source)

Mutation Taster

=100/0

polymorphism

(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

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over