rs886052706

Variant names:

• chr17-2593862-CCCCGGG-C
• rs886052706
• NM_000430.4:c.-325_-320delGGGCCC

Your query was ambiguous. Multiple possible variants found:

• chr17-2593862-CCCCGGG-C
• chr17-2593862-CCCCGGG-CCCCGGGCCCGGG

Variant summary

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

The NM_000430.4(PAFAH1B1):​c.-325_-320delGGGCCC variant causes a 5 prime UTR change. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.000014 (0 hom., cov: 0)
• Consequence: PAFAH1B1 NM_000430.4 5_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.23
• Publications: 0 publications found

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

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PAFAH1B1	NM_000430.4	c.-325_-320delGGGCCC		5_prime_UTR_variant	Exon 1 of 11	ENST00000397195.10	NP_000421.1
PAFAH1B1	XM_011523901.3	c.-325_-320delGGGCCC		5_prime_UTR_variant	Exon 1 of 12		XP_011522203.1
PAFAH1B1	XM_017024701.2	c.-191+542_-191+547delGGGCCC		intron_variant	Intron 1 of 10		XP_016880190.1
PAFAH1B1	XM_011523902.4	c.-927_-922delCCCGGG		upstream_gene_variant			XP_011522204.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PAFAH1B1	ENST00000397195.10	c.-325_-320delGGGCCC		5_prime_UTR_variant	Exon 1 of 11	1	NM_000430.4	ENSP00000380378.4

Frequencies

GnomAD3 genomes AF: 0.0000138 AC: 2 AN: 145424 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.0000506

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

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.0000138 AC: 2 AN: 145424 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 71016

African (AFR) AF: 0.0000506 AC: 2 AN: 39536

American (AMR) AF: 0.00 AC: 0 AN: 14802

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 3370

East Asian (EAS) AF: 0.00 AC: 0 AN: 4848

South Asian (SAS) AF: 0.00 AC: 0 AN: 4510

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 10050

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 298

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 65166

Other (OTH) AF: 0.00 AC: 0 AN: 1990

Alfa AF: 0.00 Hom.: 0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		4.2

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs886052706; hg19: chr17-2497156;