NM_020800.3:c.721G>A

Variant names:

• chr3-160356069-C-T
• rs138004478
• NM_020800.3:c.721G>A

Variant summary

Our verdict is Likely pathogenic. The variant received 9 ACMG points: 9P and 0B. PS1_Moderate PM2 PP3_Strong PP5

The NM_020800.3(IFT80):​c.721G>A​(p.Gly241Arg) 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 Pathogenic (no stars). Another nucleotide change resulting in the same amino acid substitution has been previously reported as Likely pathogenic in ClinVar. Synonymous variant affecting the same amino acid position (i.e. G241G) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: IFT80 NM_020800.3 missense
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 7.57
• Publications: 4 publications found

Genes affected

IFT80 (HGNC:29262): (intraflagellar transport 80) The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]

TRIM59-IFT80 (HGNC:56756): (TRIM59-IFT80 readthrough (NMD candidate)) This locus represents naturally occurring readthrough transcription between the neighboring TRIM59 (tripartite motif containing 59) and IFT80 (intraflagellar transport 80) genes on chromosome 3. The readthrough transcript is unlikely to produce a protein product. [provided by RefSeq, Jun 2017]

ACMG classification

Our verdict: Likely_pathogenic. The variant received 9 ACMG points.

• PS1: Transcript NM_020800.3 (IFT80) is affected with MISSENSE_VARIANT having same AA change as one Pathogenic present in ClinVar.
• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.971
• PP5: Variant 3-160356069-C-T is Pathogenic according to our data. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr3-160356069-C-T is described in CliVar as Pathogenic. Clinvar id is 100665.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
IFT80	NM_020800.3	c.721G>A	p.Gly241Arg	missense_variant	Exon 8 of 20	ENST00000326448.12	NP_065851.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
IFT80	ENST00000326448.12	c.721G>A	p.Gly241Arg	missense_variant	Exon 8 of 20	1	NM_020800.3	ENSP00000312778.7
TRIM59-IFT80	ENST00000483754.1	n.1234G>A		non_coding_transcript_exon_variant	Exon 6 of 19	2		ENSP00000456272.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: no assertion criteria provided

Submissions by phenotype

Asphyxiating thoracic dystrophy 2 Pathogenic:1

Feb 01, 2011

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.91
BayesDel_addAF	Pathogenic	0.32	D
BayesDel_noAF	Pathogenic	0.22
CADD	Pathogenic	31
DANN	Pathogenic	1.0
DEOGEN2	Uncertain	0.65	D;.;.;T
Eigen	Pathogenic	0.95
Eigen_PC	Pathogenic	0.88
FATHMM_MKL	Pathogenic	0.98	D
LIST_S2	Pathogenic	0.99	D;.;D;D
M_CAP	Uncertain	0.12	D
MetaRNN	Pathogenic	0.97	D;D;D;D
MetaSVM	Uncertain	-0.11	T
MutationAssessor	Pathogenic	4.4	H;.;.;.
PhyloP100		7.6
PrimateAI	Pathogenic	0.81	D
PROVEAN	Pathogenic	-7.4	D;D;D;D
REVEL	Uncertain	0.63
Sift	Pathogenic	0.0	D;D;D;D
Sift4G	Uncertain	0.0020	D;D;D;D
Polyphen		1.0	D;.;.;.
Vest4		0.98
MutPred		0.88		Gain of sheet (P = 0.1208);.;.;.;
MVP		0.81
MPC		0.73
ClinPred		1.0	D
GERP RS		5.4
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.82
gMVP		0.76
Mutation Taster		=2/98	disease causing (ClinVar)

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

Other links and lift over

dbSNP: rs138004478; hg19: chr3-160073857;