NM_145045.5:c.1060C>A

Variant names:

• chr19-11423933-G-T
• NM_145045.5:c.1060C>A

Variant summary

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

The NM_145045.5(ODAD3):​c.1060C>A​(p.Gln354Lys) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000205 in 1,461,304 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 30)
  • Exomes 𝑓: 0.0000021 (0 hom.)
• Consequence: ODAD3 NM_145045.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 3.33

Genes affected

ODAD3 (HGNC:28303): (outer dynein arm docking complex subunit 3) This gene encodes a protein containing coiled-coil domains. The encoded protein functions in outer dynein arm assembly and is required for motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]

ACMG classification

Verdict is Uncertain_significance. Variant got 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ODAD3	NM_145045.5	c.1060C>A	p.Gln354Lys	missense_variant	Exon 8 of 13	ENST00000356392.9	NP_659482.3
ODAD3	NM_001302453.1	c.898C>A	p.Gln300Lys	missense_variant	Exon 8 of 13		NP_001289382.1
ODAD3	NM_001302454.2	c.880C>A	p.Gln294Lys	missense_variant	Exon 6 of 11		NP_001289383.1
ODAD3	XM_017026241.2	c.1001C>A	p.Pro334Gln	missense_variant	Exon 8 of 9		XP_016881730.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ODAD3	ENST00000356392.9	c.1060C>A	p.Gln354Lys	missense_variant	Exon 8 of 13	1	NM_145045.5	ENSP00000348757.3

Frequencies

GnomAD3 genomes Cov.: 30

GnomAD4 exome AF: 0.00000205 AC: 3 AN: 1461304 Hom.: 0 Cov.: 34 AF XY: 0.00000138 AC XY: 1 AN XY: 726960

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: 0.00

Gnomad4 NFE exome AF: 0.00000270

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 30

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.14
BayesDel_addAF	Uncertain	0.048	T
BayesDel_noAF	Benign	-0.17
CADD	Benign	22
DANN	Benign	0.96
DEOGEN2	Benign	0.0050	T;T;.
Eigen	Benign	0.032
Eigen_PC	Benign	0.11
FATHMM_MKL	Uncertain	0.89	D
LIST_S2	Benign	0.84	T;T;T
M_CAP	Uncertain	0.14	D
MetaRNN	Uncertain	0.57	D;D;D
MetaSVM	Uncertain	-0.18	T
MutationAssessor	Uncertain	2.5	M;.;.
PrimateAI	Benign	0.44	T
PROVEAN	Benign	-1.0	N;.;.
REVEL	Uncertain	0.37
Sift	Benign	0.19	T;.;.
Sift4G	Benign	0.66	T;T;T
Polyphen		0.66	P;.;.
Vest4		0.54
MutPred		0.60		Gain of ubiquitination at Q354 (P = 0.0162);.;.;
MVP		0.73
MPC		0.68
ClinPred		0.67	D
GERP RS		4.2
Varity_R		0.21
gMVP		0.43

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: chr19-11534602;