NM_000443.4:c.2169dupG

Variant names:

Variant summary

Our verdict is Pathogenic. The variant received 11 ACMG points: 11P and 0B. PVS1PM2PP5

The NM_000443.4(ABCB4):c.2169dupG(p.Leu724AlafsTer21) variant causes a frameshift change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000274 in 1,461,802 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Pathogenic (no stars). Synonymous variant affecting the same amino acid position (i.e. G723G) has been classified as Likely benign. Variant results in nonsense mediated mRNA decay.

Frequency

Genomes: not found (cov: 32)

Exomes 𝑓: 0.0000027 ( 0 hom. )

Consequence

ABCB4
NM_000443.4 frameshift

Scores

Not classified

Clinical Significance

Pathogenic no assertion criteria provided P:1

Conservation

PhyloP100: -6.82

Publications

3 publications found

Variant links:

Genes affected

ABCB4 (HGNC:45): (ATP binding cassette subfamily B member 4) The membrane-associated 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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This gene encodes a full transporter and member of the p-glycoprotein family of membrane proteins with phosphatidylcholine as its substrate. The function of this protein has not yet been determined; however, it may involve transport of phospholipids from liver hepatocytes into bile. Alternative splicing of this gene results in several products of undetermined function. [provided by RefSeq, Jul 2008]

ABCB4 Gene-Disease associations (from GenCC):

progressive familial intrahepatic cholestasis type 3
Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), ClinGen, Orphanet
gallbladder disease 1
Inheritance: SD, AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Ambry Genetics, Labcorp Genetics (formerly Invitae), Orphanet
pancreatitis
Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics

ABCB4 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Pathogenic. The variant received 11 ACMG points.

PVS1

Loss of function variant, product undergoes nonsense mediated mRNA decay. LoF is a known mechanism of disease.

PM2

Very rare variant in population databases, with high coverage;

PP5

Variant 7-87423947-G-GC is Pathogenic according to our data. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr7-87423947-G-GC is described in CliVar as Pathogenic. Clinvar id is 13694.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ABCB4	NM_000443.4 link	c.2169dupG	p.Leu724AlafsTer21	frameshift_variant	Exon 17 of 28	ENST00000649586.2	NP_000434.1	P21439-2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ABCB4	ENST00000649586.2 link	c.2169dupG	p.Leu724AlafsTer21	frameshift_variant	Exon 17 of 28		NM_000443.4	ENSP00000496956.2		P21439-2

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

AF:

0.00000274

AC:

AN:

1461802

Hom.:

Cov.:

AF XY:

0.00000275

AC XY:

AN XY:

727210

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

33472

American (AMR)

AF:

0.00

AC:

AN:

44722

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26128

East Asian (EAS)

AF:

0.00

AC:

AN:

39696

South Asian (SAS)

AF:

0.00

AC:

AN:

86258

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53420

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5768

European-Non Finnish (NFE)

AF:

0.00000180

AC:

AN:

1111948

Other (OTH)

AF:

0.0000331

AC:

AN:

60390

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

Cov.:

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

LINK: link

Submissions by phenotype

Progressive familial intrahepatic cholestasis type 3

Pathogenic:1

Jan 06, 1998

OMIM

Significance:Pathogenic

Review Status:no assertion criteria provided

Collection Method:literature only

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

PhyloP100

-6.8

Mutation Taster

=0/200

disease causing (ClinVar)

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.090

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