NM_020297.4:c.1165-2A>G

Variant names:

Variant summary

Our verdict is Likely pathogenic. The variant received 6 ACMG points: 6P and 0B. PVS1_ModeratePM2PP5_Moderate

The NM_020297.4(ABCC9):c.1165-2A>G variant causes a splice acceptor, intron change involving the alteration of a conserved nucleotide. The variant allele was found at a frequency of 0.00000213 in 1,409,180 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a pathogenic outcome for this variant. 3/3 splice prediction tools predicting alterations to normal splicing. Variant has been reported in ClinVar as Likely pathogenic (★).

Frequency

Genomes: 𝑓 0.0 ( 0 hom., cov: 30)

Exomes 𝑓: 0.0000021 ( 0 hom. )

Failed GnomAD Quality Control

Consequence

ABCC9
NM_020297.4 splice_acceptor, intron

Scores

Splicing: ADA: 0.9999

Clinical Significance

Likely pathogenic criteria provided, single submitter P:1

Conservation

PhyloP100: 8.00

Publications

0 publications found

Variant links:

Genes affected

ABCC9 (HGNC:60): (ATP binding cassette subfamily C member 9) The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein is thought to form ATP-sensitive potassium channels in cardiac, skeletal, and vascular and non-vascular smooth muscle. Protein structure suggests a role as the drug-binding channel-modulating subunit of the extra-pancreatic ATP-sensitive potassium channels. Mutations in this gene are associated with cardiomyopathy dilated type 1O. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011]

ABCC9 Gene-Disease associations (from GenCC):

hypertrichotic osteochondrodysplasia Cantu type
Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Orphanet, G2P, Labcorp Genetics (formerly Invitae), Ambry Genetics
dilated cardiomyopathy 1O
Inheritance: AD Classification: STRONG, MODERATE, LIMITED Submitted by: Illumina, Ambry Genetics, Labcorp Genetics (formerly Invitae)
intellectual disability and myopathy syndrome
Inheritance: AR Classification: MODERATE, LIMITED Submitted by: Ambry Genetics, Labcorp Genetics (formerly Invitae)
acromegaloid facial appearance syndrome
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
familial isolated dilated cardiomyopathy
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
hypertrichosis-acromegaloid facial appearance syndrome
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
Brugada syndrome
Inheritance: AD Classification: LIMITED Submitted by: Genomics England PanelApp
dilated cardiomyopathy
Inheritance: AD Classification: LIMITED Submitted by: ClinGen
atrial fibrillation, familial, 12
Inheritance: Unknown Classification: LIMITED Submitted by: Labcorp Genetics (formerly Invitae)

ABCC9 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Likely_pathogenic. The variant received 6 ACMG points.

PVS1

Splicing +-2 bp (donor or acceptor) variant, product NOT destroyed by NMD, known LOF gene, truncates exone, which is 0.03354839 fraction of the gene. Cryptic splice site detected, with MaxEntScore 3.9, offset of 26, new splice context is: atttataataaaatccttAGgct. Cryptic site results in frameshift change. If cryptic site found is not functional and variant results in exon loss, it results in inframe change.

PM2

Very rare variant in population databases, with high coverage;

PP5

Variant 12-21910314-T-C is Pathogenic according to our data. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr12-21910314-T-C is described in CliVar as Likely_pathogenic. Clinvar id is 240201.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ABCC9	NM_020297.4 link	c.1165-2A>G		splice_acceptor_variant, intron_variant	Intron 9 of 39	ENST00000261200.9	NP_064693.2	O60706-2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ABCC9	ENST00000261200.9 link	c.1165-2A>G		splice_acceptor_variant, intron_variant	Intron 9 of 39	5	NM_020297.4	ENSP00000261200.4		O60706-2

Frequencies

GnomAD3 genomes

AF:

0.00

AC:

AN:

114344

Hom.:

Cov.:

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:

0.00

Gnomad OTH

AF:

0.00

GnomAD2 exomes

AF:

0.00000550

AC:

AN:

181938

AF XY:

0.00

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:

0.0000114

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.00000213

AC:

AN:

1409180

Hom.:

Cov.:

AF XY:

0.00000143

AC XY:

AN XY:

701382

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

30158

American (AMR)

AF:

0.00

AC:

AN:

35934

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

24588

East Asian (EAS)

AF:

0.00

AC:

AN:

38668

South Asian (SAS)

AF:

0.00

AC:

AN:

79612

European-Finnish (FIN)

AF:

0.00

AC:

AN:

45600

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5258

European-Non Finnish (NFE)

AF:

0.00000275

AC:

AN:

1091332

Other (OTH)

AF:

0.00

AC:

AN:

58030

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

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

Data not reliable, filtered out with message: AC0

AF:

0.00

AC:

AN:

114344

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

54880

African (AFR)

AF:

0.00

AC:

AN:

31582

American (AMR)

AF:

0.00

AC:

AN:

10586

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

2996

East Asian (EAS)

AF:

0.00

AC:

AN:

4536

South Asian (SAS)

AF:

0.00

AC:

AN:

3690

European-Finnish (FIN)

AF:

0.00

AC:

AN:

6042

Middle Eastern (MID)

AF:

0.00

AC:

AN:

242

European-Non Finnish (NFE)

AF:

0.00

AC:

AN:

52474

Other (OTH)

AF:

0.00

AC:

AN:

1540

Alfa

AF:

0.00

Hom.:

ClinVar

Significance: Likely pathogenic

Submissions summary: Pathogenic:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

Dilated cardiomyopathy 1O

Pathogenic:1

Oct 01, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Likely pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

This sequence change affects an acceptor splice site in intron 7 of the ABCC9 gene. It is expected to disrupt RNA splicing. Variants that disrupt the donor or acceptor splice site typically lead to a loss of protein function (PMID: 16199547), and loss-of-function variants in ABCC9 are known to be pathogenic (PMID: 31575858, 38217872). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with ABCC9-related conditions. ClinVar contains an entry for this variant (Variation ID: 240201). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_addAF

Pathogenic

0.24

BayesDel_noAF

Uncertain

0.10

CADD

Pathogenic

(source)

DANN

Uncertain

0.99

Eigen

Pathogenic

1.0

Eigen_PC

Pathogenic

0.85

FATHMM_MKL

Pathogenic

0.99

PhyloP100

8.0

GERP RS

5.5

Mutation Taster

=0/100

disease causing

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

dbscSNV1_ADA

Pathogenic

1.0

dbscSNV1_RF

Pathogenic

0.94

SpliceAI score (max)

0.97

Details are displayed if max score is > 0.2

DS_AG_spliceai

0.31

Position offset: -28

DS_AL_spliceai

0.97

Position offset: -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

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over