chr19-40757355-A-G

Position:

• chr19-40757355-A-G

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 4P and 3B. PM2 PM5 BP4 BP6_Moderate

The NM_004596.5(SNRPA):​c.97A>G​(p.Ile33Val) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 12/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. I33T) has been classified as Likely pathogenic.

• Frequency: Genomes: not found (cov: 31)
• Consequence: SNRPA NM_004596.5 missense
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 5.01

Genes affected

SNRPA (HGNC:11151): (small nuclear ribonucleoprotein polypeptide A) The protein encoded by this gene associates with stem loop II of the U1 small nuclear ribonucleoprotein, which binds the 5' splice site of precursor mRNAs and is required for splicing. The encoded protein autoregulates itself by polyadenylation inhibition of its own pre-mRNA via dimerization and has been implicated in the coupling of splicing and polyadenylation. [provided by RefSeq, Oct 2010]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PM5: Other missense variant is known to change same aminoacid residue: Variant chr19-40757356-T-C is described in ClinVar as [Likely_pathogenic]. Clinvar id is 446220.Status of the report is criteria_provided_single_submitter, 1 stars.
• BP4: Computational evidence support a benign effect (MetaRNN=0.30744287).
• BP6: Variant 19-40757355-A-G is Benign according to our data. Variant chr19-40757355-A-G is described in ClinVar as [Likely_benign]. Clinvar id is 446221.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SNRPA	NM_004596.5	c.97A>G	p.Ile33Val	missense_variant	2/6	ENST00000243563.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SNRPA	ENST00000243563.8	c.97A>G	p.Ile33Val	missense_variant	2/6	1	NM_004596.5	P1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 31

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Spliceosomepathy Benign:1

Likely benign, criteria provided, single submitter

research

Laboratorio de Citogenómica y Microarreglos, Universidad Autonoma de Nuevo Leon

Nov 01, 2017

Splicing-related gene mutations might affect in different ways the expression of a single gene or multiple genes. Exome sequencing analyses by Variant Interpreter identified, in independent assays of the patients, three homozygous missense variants in exon 2 of SNRPA (hg19; chr19:41,263,260, chr19:41,263,261, and chr19:41,263,263; NM_004596.4). These variants were described as c.97A>G, c.98T>C, and c.100T>A and cause a change in two contiguous amino acids: p.Ile33Ala and p.Phe34Ile. The in-silico analyses (CFSSP, ExPASy web tool) showed a gained rich-α-helix region. Six different bioinformatic platforms predicted a pathogenic consequence for p.Ile33Ala and p.Phe34Ile; however, a more pathogenic score (-8.53, PROVEAN web tool) was predicted when both mutations were analyzed combined. SNRPA encodes for a protein that associates with the stem loop II of the U1 RNA. SNRPA/U1-A along with SNRNP70/U1-70K, SNRPC/U1-C and a core of proteins known as Sm, conform the U1 small nuclear ribonucleoprotein complex. The PD/ID and growth, eye, craniofacial and hand anomalies in our patients, are features also seen in other spliceosomepathies. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.68
BayesDel_addAF	Benign	-0.14	T
BayesDel_noAF	Benign	-0.43
CADD	Benign	22
DANN	Benign	0.97
DEOGEN2	Benign	0.10	T;.;T;.;.
Eigen	Benign	-0.23
Eigen_PC	Benign	0.0041
FATHMM_MKL	Uncertain	0.89	D
LIST_S2	Uncertain	0.93	D;D;D;D;D
M_CAP	Benign	0.0092	T
MetaRNN	Benign	0.31	T;T;T;T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	0.19	N;.;.;.;.
MutationTaster	Benign	1.0	D
PrimateAI	Uncertain	0.71	T
PROVEAN	Benign	-0.52	N;.;.;.;.
REVEL	Benign	0.15
Sift	Benign	0.62	T;.;.;.;.
Sift4G	Benign	0.63	T;T;T;T;T
Polyphen		0.0	B;.;.;.;.
Vest4		0.48
MutPred		0.60		Loss of stability (P = 0.104);Loss of stability (P = 0.104);Loss of stability (P = 0.104);Loss of stability (P = 0.104);Loss of stability (P = 0.104);
MVP		0.42
MPC		0.55
ClinPred		0.37	T
GERP RS		4.8
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.26
gMVP		0.17

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

LitVar

Other links and lift over

dbSNP: rs1555775207; hg19: chr19-41263260;