NM_001367479.1:c.3032G>T

Variant names:

• chr1-225080644-G-T
• rs3128652
• NM_001367479.1:c.3032G>T

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001367479.1(DNAH14):​c.3032G>T​(p.Arg1011Leu) 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. 14/17 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. R1011Q) has been classified as Benign.

• Frequency: Genomes: not found (cov: 33)
• Consequence: DNAH14 NM_001367479.1 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.59

Genes affected

DNAH14 (HGNC:2945): (dynein axonemal heavy chain 14) Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. Two major classes of dyneins, axonemal and cytoplasmic, have been identified. DNAH14 is an axonemal dynein heavy chain (DHC) (Vaughan et al., 1996 [PubMed 8812413]).[supplied by OMIM, Mar 2008]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.052168578).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DNAH14	NM_001367479.1	c.3032G>T	p.Arg1011Leu	missense_variant	Exon 19 of 86	ENST00000682510.1	NP_001354408.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DNAH14	ENST00000682510.1	c.3032G>T	p.Arg1011Leu	missense_variant	Exon 19 of 86		NM_001367479.1	ENSP00000508305.1
DNAH14	ENST00000430092.5	c.3032G>T	p.Arg1011Leu	missense_variant	Exon 19 of 84	5		ENSP00000414402.1
DNAH14	ENST00000439375.6	c.3032G>T	p.Arg1011Leu	missense_variant	Exon 18 of 83	5		ENSP00000392061.2
DNAH14	ENST00000445597.6	c.2834G>T	p.Arg945Leu	missense_variant	Exon 15 of 61	5		ENSP00000409472.2

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 55

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.095
BayesDel_addAF	Benign	-0.25	T
BayesDel_noAF	Benign	-0.60
CADD	Benign	0.015
DANN	Benign	0.89
DEOGEN2	Benign	0.0067	T;.;.
Eigen	Benign	-1.9
Eigen_PC	Benign	-1.9
FATHMM_MKL	Benign	0.0071	N
LIST_S2	Benign	0.27	T;T;.
M_CAP	Benign	0.054	D
MetaRNN	Benign	0.052	T;T;T
MetaSVM	Benign	-1.0	T
PrimateAI	Benign	0.29	T
PROVEAN	Benign	-1.4	N;N;N
REVEL	Benign	0.019
Sift	Benign	0.14	T;T;T
Sift4G	Benign	0.12	T;T;T
Polyphen		0.0	.;B;B
Vest4		0.13
MutPred		0.46		.;Loss of MoRF binding (P = 0.0102);Loss of MoRF binding (P = 0.0102);
MVP		0.16
ClinPred		0.068	T
GERP RS		-6.7
Varity_R		0.039

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: rs3128652; hg19: chr1-225268346;