Variant 19-3492299-G-T details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Uncertain significance. Variant got 3 ACMG points: 3P and 0B. PM2PP5

The NM_001145165.2(DOHH):c.552C>A(p.Asn184Lys) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000073 in 1,369,728 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Pathogenic (no stars).

Frequency

Genomes: not found (cov: 33)

Exomes 𝑓: 7.3e-7 ( 0 hom. )

Consequence

DOHH
NM_001145165.2 missense

Scores

Clinical Significance

Pathogenic no assertion criteria provided P:2

Conservation

PhyloP100: 0.170

Variant links:

Genes affected

DOHH (HGNC:28662): (deoxyhypusine hydroxylase) This gene encodes a metalloenzyme that catalyzes the last step in the conversion of lysine to the unique amino acid hypusine in eukaryotic initiation factor 5A. The encoded protein hydroxylates deoxyhypusine to form hypusine in the mature eukaryotic initiation factor 5A protein. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009]

DOHH links:

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ACMG classification

Classification made for transcript

Verdict is Uncertain_significance. Variant got 3 ACMG points.

PM2

Very rare variant in population databases, with high coverage;

PP5

Variant 19-3492299-G-T is Pathogenic according to our data. Variant chr19-3492299-G-T is described in ClinVar as [Pathogenic]. Clinvar id is 1285605.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr19-3492299-G-T is described in Lovd as [Likely_pathogenic].

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
DOHH	NM_001145165.2 link	c.552C>A	p.Asn184Lys	missense_variant	4/5	ENST00000427575.6	NP_001138637.1
DOHH	NM_031304.5 link	c.552C>A	p.Asn184Lys	missense_variant	4/5		NP_112594.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	UniProt
DOHH	ENST00000427575.6 link	c.552C>A	p.Asn184Lys	missense_variant	4/5	1	NM_001145165.2	ENSP00000398882.1	Q9BU89
DOHH	ENST00000672935.1 link	c.552C>A	p.Asn184Lys	missense_variant	4/5			ENSP00000500806.1	Q9BU89
DOHH	ENST00000671696.1 link	c.405C>A	p.Asn135Lys	missense_variant	3/3			ENSP00000499813.1	A0A5F9ZGM7
DOHH	ENST00000673168.1 link	n.345C>A		non_coding_transcript_exon_variant	2/3

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

AF:

7.30e-7

AC:

AN:

1369728

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

676642

show subpopulations

Gnomad4 AFR exome

AF:

0.00

Gnomad4 AMR exome

AF:

0.00

Gnomad4 ASJ exome

AF:

0.00

Gnomad4 EAS exome

AF:

0.00

Gnomad4 SAS exome

AF:

0.00

Gnomad4 FIN exome

AF:

0.0000279

Gnomad4 NFE exome

AF:

0.00

Gnomad4 OTH exome

AF:

0.00

GnomAD4 genome

Cov.:

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:2

Revision: no assertion criteria provided

LINK: link

Submissions by phenotype

DOHH related neurodevelopmental disorder

Pathogenic:1

Pathogenic, no assertion criteria provided

research

Department of Genetics, CHU d'Angers

Sep 22, 2021

- -

Neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment

Pathogenic:1

Pathogenic, no assertion criteria provided

literature only

OMIM

Sep 30, 2022

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Pathogenic

0.80

BayesDel_addAF

Benign

-0.17

BayesDel_noAF

Benign

-0.48

CADD

Benign

7.9

DANN

Benign

0.89

DEOGEN2

Benign

0.35

Eigen

Benign

-1.0

Eigen_PC

Benign

-1.4

FATHMM_MKL

Benign

0.068

LIST_S2

Pathogenic

0.98

M_CAP

Benign

0.066

MetaRNN

Uncertain

0.49

MetaSVM

Uncertain

-0.045

MutationAssessor

Pathogenic

3.5

PrimateAI

Uncertain

0.71

PROVEAN

Pathogenic

-5.6

REVEL

Uncertain

0.35

Sift

Uncertain

0.0030

Sift4G

Uncertain

0.0030

Polyphen

0.98

Vest4

0.23

MutPred

0.65

Gain of ubiquitination at N184 (P = 0.017);

MVP

0.13

MPC

1.1

ClinPred

0.91

GERP RS

-8.7

Varity_R

0.74

gMVP

0.26

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

No publications associated with this variant yet.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over