5-31410829-C-T

Position:

• chr5-31410829-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 4 ACMG points: 4P and 0B. PM2 PP3_Moderate

The NM_001382508.1(DROSHA):​c.3584G>A​(p.Gly1195Asp) 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 Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: DROSHA NM_001382508.1 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 7.46

Genes affected

DROSHA (HGNC:17904): (drosha ribonuclease III) This gene encodes a ribonuclease (RNase) III double-stranded RNA-specific ribonuclease and subunit of the microprocessor protein complex, which catalyzes the initial processing step of microRNA (miRNA) synthesis. The encoded protein cleaves the stem loop structure from the primary microRNA (pri-miRNA) in the nucleus, yielding the precursor miRNA (pre-miRNA), which is then exported to the cytoplasm for further processing. In a human cell line lacking a functional copy of this gene, canonical miRNA synthesis is reduced. Somatic mutations in this gene have been observed in human patients with kidney cancer. [provided by RefSeq, Sep 2016]

DROSHA (HGNC:):

ACMG classification

Verdict is Uncertain_significance. Variant got 4 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.873

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
DROSHA	NM_001382508.1	c.3584G>A	p.Gly1195Asp	missense_variant	31/36	ENST00000344624.8	NP_001369437.1
DROSHA	NM_013235.5	c.3584G>A	p.Gly1195Asp	missense_variant	30/35		NP_037367.3
DROSHA	NM_001100412.2	c.3473G>A	p.Gly1158Asp	missense_variant	30/35		NP_001093882.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
DROSHA	ENST00000344624.8	c.3584G>A	p.Gly1195Asp	missense_variant	31/36	5	NM_001382508.1	ENSP00000339845.3
DROSHA	ENST00000511367.6	c.3584G>A	p.Gly1195Asp	missense_variant	30/35	1		ENSP00000425979.2
DROSHA	ENST00000513349.5	c.3473G>A	p.Gly1158Asp	missense_variant	30/35	1		ENSP00000424161.1
DROSHA	ENST00000511778.5	n.700G>A		non_coding_transcript_exon_variant	3/8	3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 32

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Ambry Genetics

Mar 15, 2024

The c.3584G>A (p.G1195D) alteration is located in exon 30 (coding exon 28) of the DROSHA gene. This alteration results from a G to A substitution at nucleotide position 3584, causing the glycine (G) at amino acid position 1195 to be replaced by an aspartic acid (D). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.80
BayesDel_addAF	Pathogenic	0.26	D
BayesDel_noAF	Pathogenic	0.14
CADD	Pathogenic	28
DANN	Uncertain	1.0
DEOGEN2	Uncertain	0.61	D;.;D;.
Eigen	Uncertain	0.63
Eigen_PC	Uncertain	0.66
FATHMM_MKL	Pathogenic	0.98	D
LIST_S2	Uncertain	0.96	.;D;D;.
M_CAP	Benign	0.038	D
MetaRNN	Pathogenic	0.87	D;D;D;D
MetaSVM	Benign	-0.73	T
MutationAssessor	Benign	1.8	L;.;L;.
PrimateAI	Pathogenic	0.96	D
PROVEAN	Pathogenic	-6.0	D;D;D;D
REVEL	Uncertain	0.52
Sift	Benign	0.066	T;D;T;D
Sift4G	Uncertain	0.025	D;D;D;D
Polyphen		0.93	P;.;P;.
Vest4		0.92
MutPred		0.63		Gain of sheet (P = 0.1208);.;Gain of sheet (P = 0.1208);.;
MVP		0.84
MPC		2.5
ClinPred		0.99	D
GERP RS		5.3
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.87
gMVP		0.95

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		Details are displayed if max score is > 0.2

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr5-31410936;