17-2676507-TAAAA-TAAA

Variant names:

Variant summary

Our verdict is Pathogenic. The variant received 10 ACMG points: 10P and 0B. PVS1PP5_Moderate

The NM_000430.4(PAFAH1B1):c.910delA(p.Ser304ValfsTer29) variant causes a frameshift change involving the alteration of a conserved nucleotide. The variant allele was found at a frequency of 0.00000621 in 1,449,668 control chromosomes in the GnomAD database, with no homozygous occurrence. There is a variant allele frequency bias in the population database for this variant (GnomAdExome4), which may indicate mosaicism or somatic mutations in the reference population data. Variant has been reported in ClinVar as Pathogenic (★). Variant results in nonsense mediated mRNA decay.

Frequency

Genomes: not found (cov: 33)

Exomes 𝑓: 0.0000062 ( 0 hom. )

Consequence

PAFAH1B1
NM_000430.4 frameshift

Scores

Not classified

Clinical Significance

Pathogenic criteria provided, single submitter P:1

Conservation

PhyloP100: 9.32

Publications

4 publications found

Variant links:

Genes affected

PAFAH1B1 (HGNC:8574): (platelet activating factor acetylhydrolase 1b regulatory subunit 1) This locus was identified as encoding a gene that when mutated or lost caused the lissencephaly associated with Miller-Dieker lissencephaly syndrome. This gene encodes the non-catalytic alpha subunit of the intracellular Ib isoform of platelet-activating factor acteylhydrolase, a heterotrimeric enzyme that specifically catalyzes the removal of the acetyl group at the SN-2 position of platelet-activating factor (identified as 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine). Two other isoforms of intracellular platelet-activating factor acetylhydrolase exist: one composed of multiple subunits, the other, a single subunit. In addition, a single-subunit isoform of this enzyme is found in serum. [provided by RefSeq, Apr 2009]

PAFAH1B1 Gene-Disease associations (from GenCC):

lissencephaly due to LIS1 mutation
Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: PanelApp Australia, Labcorp Genetics (formerly Invitae), G2P

PAFAH1B1 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Pathogenic. The variant received 10 ACMG points.

PVS1

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

PP5

Variant 17-2676507-TA-T is Pathogenic according to our data. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr17-2676507-TA-T is described in CliVar as Pathogenic. Clinvar id is 159551.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PAFAH1B1	NM_000430.4 link	c.910delA	p.Ser304ValfsTer29	frameshift_variant	Exon 9 of 11	ENST00000397195.10	NP_000421.1	P43034-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PAFAH1B1	ENST00000397195.10 link	c.910delA	p.Ser304ValfsTer29	frameshift_variant	Exon 9 of 11	1	NM_000430.4	ENSP00000380378.4		P43034-1

Frequencies

GnomAD3 genomes

Cov.:

GnomAD2 exomes

AF:

0.00

AC:

AN:

251346

AF XY:

0.00

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:

0.00

Gnomad OTH exome

AF:

0.00

GnomAD4 exome

AF:

0.00000621

AC:

AN:

1449668

Hom.:

Cov.:

AF XY:

0.00000692

AC XY:

AN XY:

722110

show subpopulations

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

African (AFR)

AF:

0.00

AC:

AN:

33200

American (AMR)

AF:

0.00

AC:

AN:

44712

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26050

East Asian (EAS)

AF:

0.00

AC:

AN:

39612

South Asian (SAS)

AF:

0.00

AC:

AN:

85998

European-Finnish (FIN)

AF:

0.00

AC:

AN:

53394

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5106

European-Non Finnish (NFE)

AF:

0.00000817

AC:

AN:

1101662

Other (OTH)

AF:

0.00

AC:

AN:

59934

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 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: 0.225

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: criteria provided, single submitter

LINK: link

Submissions by phenotype

Lissencephaly due to LIS1 mutation

Pathogenic:1

May 22, 2013

Genetic Services Laboratory, University of Chicago

Significance:Pathogenic

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

PhyloP100

9.3

Mutation Taster

=2/198

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

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

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