17-7733279-G-T

Position:

• chr17-7733279-G-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_020877.5(DNAH2):​c.592G>T​(p.Ala198Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 31)
• Consequence: DNAH2 NM_020877.5 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 0.908

Genes affected

DNAH2 (HGNC:2948): (dynein axonemal heavy chain 2) Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. The axonemal dyneins, found in cilia and flagella, are components of the outer and inner dynein arms attached to the peripheral microtubule doublets. DNAH2 is an axonemal inner arm dynein heavy chain (Chapelin et al., 1997 [PubMed 9256245]).[supplied by OMIM, Mar 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.08558187).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
DNAH2	NM_020877.5	c.592G>T	p.Ala198Ser	missense_variant	5/86	ENST00000572933.6	NP_065928.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
DNAH2	ENST00000572933.6	c.592G>T	p.Ala198Ser	missense_variant	5/86	2	NM_020877.5	ENSP00000458355.1
DNAH2	ENST00000570791.5	c.592G>T	p.Ala198Ser	missense_variant	5/14	1		ENSP00000460245.1
DNAH2	ENST00000389173.6	c.592G>T	p.Ala198Ser	missense_variant	4/85	2		ENSP00000373825.2

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 31

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

Inborn genetic diseases Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Ambry Genetics

Feb 22, 2023

The c.592G>T (p.A198S) alteration is located in exon 4 (coding exon 4) of the DNAH2 gene. This alteration results from a G to T substitution at nucleotide position 592, causing the alanine (A) at amino acid position 198 to be replaced by a serine (S). 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	Benign	0.089
BayesDel_addAF	Benign	-0.24	T
BayesDel_noAF	Benign	-0.59
CADD	Benign	15
DANN	Benign	0.85
DEOGEN2	Benign	0.011	T;.;T
Eigen	Benign	-0.67
Eigen_PC	Benign	-0.46
FATHMM_MKL	Benign	0.57	D
LIST_S2	Benign	0.61	.;T;T
M_CAP	Benign	0.0029	T
MetaRNN	Benign	0.086	T;T;T
MetaSVM	Benign	-0.98	T
MutationAssessor	Benign	-0.58	N;N;N
PrimateAI	Benign	0.27	T
PROVEAN	Benign	0.0	.;.;N
REVEL	Benign	0.079
Sift	Benign	0.56	.;.;T
Sift4G	Benign	0.97	.;T;.
Polyphen		0.0010	B;B;B
Vest4		0.25
MutPred		0.55		Gain of disorder (P = 0.012);Gain of disorder (P = 0.012);Gain of disorder (P = 0.012);
MVP		0.24
MPC		0.16
ClinPred		0.086	T
GERP RS		0.85
Varity_R		0.035
gMVP		0.14

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.

Other links and lift over

hg19: chr17-7636597;