chr11-126265094-G-C

Position:

• chr11-126265094-G-C

Variant summary

Our verdict is Likely pathogenic. Variant got 7 ACMG points: 7P and 0B. PM2 PP3_Strong PP5

The NM_003139.4(SRPRA):​c.1390C>G​(p.Gln464Glu) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Pathogenic (no stars).

• Frequency: Genomes: not found (cov: 33)
• Consequence: SRPRA NM_003139.4 missense
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 9.53

Genes affected

SRPRA (HGNC:11307): (SRP receptor subunit alpha) The gene encodes a subunit of the endoplasmic reticulum signal recognition particle receptor that, in conjunction with the signal recognition particle, is involved in the targeting and translocation of signal sequence tagged secretory and membrane proteins across the endoplasmic reticulum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010]

ACMG classification

Verdict is Likely_pathogenic. Variant got 7 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.959
• PP5: Variant 11-126265094-G-C is Pathogenic according to our data. Variant chr11-126265094-G-C is described in ClinVar as [Pathogenic]. Clinvar id is 810840.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SRPRA	NM_003139.4	c.1390C>G	p.Gln464Glu	missense_variant	11/14	ENST00000332118.11	NP_003130.2
SRPRA	NM_001177842.2	c.1306C>G	p.Gln436Glu	missense_variant	10/13		NP_001171313.1
SRPRA	XM_047427497.1	c.1390C>G	p.Gln464Glu	missense_variant	11/14		XP_047283453.1
SRPRA	XM_017018179.3	c.1390C>G	p.Gln464Glu	missense_variant	11/14		XP_016873668.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SRPRA	ENST00000332118.11	c.1390C>G	p.Gln464Glu	missense_variant	11/14	1	NM_003139.4	ENSP00000328023.5
SRPRA	ENST00000532259.1	c.1306C>G	p.Gln436Glu	missense_variant	10/13	2		ENSP00000435508.1
SRPRA	ENST00000527817.1	n.673C>G		non_coding_transcript_exon_variant	5/5	2
SRPRA	ENST00000531104.1	n.469C>G		non_coding_transcript_exon_variant	2/2	2

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 33

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Severe congenital neutropenia;C4692625:Shwachman-Diamond syndrome 1 Pathogenic:1

Pathogenic, no assertion criteria provided

research

Genomics Facility, Ludwig-Maximilians-Universität München

Jan 06, 2020

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.96
BayesDel_addAF	Pathogenic	0.50	D
BayesDel_noAF	Pathogenic	0.47
CADD	Pathogenic	30
DANN	Uncertain	1.0
DEOGEN2	Uncertain	0.68	D;.
Eigen	Pathogenic	1.2
Eigen_PC	Pathogenic	1.0
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Pathogenic	0.99	D;D
M_CAP	Uncertain	0.13	D
MetaRNN	Pathogenic	0.96	D;D
MetaSVM	Pathogenic	0.82	D
PrimateAI	Pathogenic	0.82	D
PROVEAN	Uncertain	-2.9	D;D
REVEL	Pathogenic	0.91
Sift	Uncertain	0.0030	D;D
Sift4G	Pathogenic	0.0	D;D
Polyphen		1.0	D;.
Vest4		0.92
MutPred		0.88		Gain of disorder (P = 0.052);.;
MVP		0.72
MPC		1.3
ClinPred		1.0	D
GERP RS		5.3
Varity_R		0.98
gMVP		0.97

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: rs1950780024; hg19: chr11-126134989;