NM_014845.6:c.290-2A>T

Variant names:

• chr6-109727107-A-T
• rs587777715
• NM_014845.6:c.290-2A>T

Variant summary

Our verdict is Pathogenic. The variant received 10 ACMG points: 10P and 0B. PVS1 PP5_Moderate

The NM_014845.6(FIG4):​c.290-2A>T variant causes a splice acceptor, intron change involving the alteration of a conserved nucleotide. The variant allele was found at a frequency of 0.0000117 in 1,454,228 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: not found (cov: 32)
  • Exomes 𝑓: 0.000012 (0 hom.)
• Consequence: FIG4 NM_014845.6 splice_acceptor, intron
• Scores: Splicing: ADA: 1.000
• Clinical Significance: Likely pathogenic criteria provided, single submitter P:2 U:2
• Conservation: PhyloP100: 8.97
• Publications: 1 publications found

Genes affected

FIG4 (HGNC:16873): (FIG4 phosphoinositide 5-phosphatase) The protein encoded by this gene belongs to the SAC domain-containing protein gene family. The SAC domain, approximately 400 amino acids in length and consisting of seven conserved motifs, has been shown to possess phosphoinositide phosphatase activity. The yeast homolog, Sac1p, is involved in the regulation of various phosphoinositides, and affects diverse cellular functions such as actin cytoskeleton organization, Golgi function, and maintenance of vacuole morphology. Membrane-bound phosphoinositides function as signaling molecules and play a key role in vesicle trafficking in eukaryotic cells. Mutations in this gene have been associated with Charcot-Marie-Tooth disease, type 4J. [provided by RefSeq, Jul 2008]

FIG4 Gene-Disease associations (from GenCC):

• Charcot-Marie-Tooth disease

  Inheritance: AR Classification: DEFINITIVE Submitted by: ClinGen, Illumina
• Charcot-Marie-Tooth disease type 4J

  Inheritance: AR Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), Orphanet, Ambry Genetics, Laboratory for Molecular Medicine
• Yunis-Varon syndrome

  Inheritance: AR Classification: STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), Orphanet, G2P
• amyotrophic lateral sclerosis type 11

  Inheritance: Unknown, AD Classification: STRONG, LIMITED Submitted by: Labcorp Genetics (formerly Invitae), ClinGen, Genomics England PanelApp
• amyotrophic lateral sclerosis

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• bilateral parasagittal parieto-occipital polymicrogyria

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

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

• PVS1: Splicing +-2 bp (donor or acceptor) variant, LoF is a know mechanism of disease, Cryptic splice site detected, with MaxEntScore 6.6, offset of 10, new splice context is: tgttgcattggttttgtcAGgtt. Cryptic site results in frameshift change. If cryptic site found is not functional and variant results in exon loss, it results in frameshift change.
• PP5: Variant 6-109727107-A-T is Pathogenic according to our data. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chr6-109727107-A-T is described in CliVar as Likely_pathogenic. Clinvar id is 156016.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FIG4	NM_014845.6	c.290-2A>T		splice_acceptor_variant, intron_variant	Intron 3 of 22	ENST00000230124.8	NP_055660.1
FIG4	XM_011536281.4	c.227-2A>T		splice_acceptor_variant, intron_variant	Intron 3 of 22		XP_011534583.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FIG4	ENST00000230124.8	c.290-2A>T		splice_acceptor_variant, intron_variant	Intron 3 of 22	1	NM_014845.6	ENSP00000230124.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD2 exomes AF: 0.0000120 AC: 3 AN: 251018 AF XY: 0.0000147

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: 0.0000264

Gnomad OTH exome AF: 0.00

GnomAD4 exome AF: 0.0000117 AC: 17 AN: 1454228 Hom.: 0 Cov.: 29 AF XY: 0.00000967 AC XY: 7 AN XY: 724060

African (AFR) AF: 0.00 AC: 0 AN: 33342

American (AMR) AF: 0.00 AC: 0 AN: 44684

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 26044

East Asian (EAS) AF: 0.00 AC: 0 AN: 39636

South Asian (SAS) AF: 0.00 AC: 0 AN: 86090

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 53400

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 5718

European-Non Finnish (NFE) AF: 0.0000145 AC: 16 AN: 1105184

Other (OTH) AF: 0.0000166 AC: 1 AN: 60130

GnomAD4 genome Cov.: 32

Alfa AF: 0.00 Hom.: 0

ExAC AF: 0.0000165 AC: 2

EpiCase AF: 0.00

EpiControl AF: 0.0000593

ClinVar

Significance: Likely pathogenic

Submissions summary: Pathogenic:2 Uncertain:2

Revision: criteria provided, single submitter

Submissions by phenotype

Charcot-Marie-Tooth disease type 4J Pathogenic:2 Uncertain:1

Aug 01, 2014

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

- -

Jun 13, 2023

Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Significance: Likely pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Variant summary: FIG4 c.290-2A>T is located in a canonical splice-site and is predicted to affect mRNA splicing resulting in a significantly altered protein due to either exon skipping, shortening, or inclusion of intronic material. Several computational tools predict a significant impact on normal splicing: Four predict the variant abolishes the canonical 3' splicing acceptor site and three predict it strengthens an alternate 3' splicing acceptor site located in the adjacent exon 4. However, these predictions have yet to be confirmed by functional studies. The variant allele was found at a frequency of 1.2e-05 in 251018 control chromosomes. c.290-2A>T has been reported in the literature as a biallelic compound heterozygous genotype in at least one individual affected with Charcot-Marie Disease Type 4J (e.g., Menezes_2014). To our knowledge, no experimental evidence demonstrating an impact on protein function has been reported. The following publication have been ascertained in the context of this evaluation (PMID: 24878229). One ClinVar submitter has submitted clinical-significance assessments for this variant to ClinVar after 2014 and classified the variant as a variant of uncertain significance citing overlapping evidence utilized in the context of this evaluation. Based on the evidence outlined above, the variant was classified as likely pathogenic. -

Jan 06, 2016

Inherited Neuropathy Consortium Ii, University Of Miami

Significance: Uncertain significance

Review Status: no assertion criteria provided

Collection Method: literature only

- -

Charcot-Marie-Tooth disease Uncertain:1

-

Inherited Neuropathy Consortium

Significance: Uncertain significance

Review Status: no assertion criteria provided

Collection Method: literature only

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Pathogenic	0.58	D
BayesDel_noAF	Pathogenic	0.20
CADD	Pathogenic	32
DANN	Uncertain	1.0
Eigen	Pathogenic	1.1
Eigen_PC	Pathogenic	0.94
FATHMM_MKL	Pathogenic	0.99	D
PhyloP100		9.0
GERP RS		5.0
Mutation Taster		=0/100	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Pathogenic	1.0
dbscSNV1_RF	Pathogenic	0.93
SpliceAI score (max)		0.72		Details are displayed if max score is > 0.2
DS_AG_spliceai		0.40		Position offset: 12
DS_AL_spliceai		0.72		Position offset: 2

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

Other links and lift over

dbSNP: rs587777715; hg19: chr6-110048310; COSMIC: COSV57787190;