rs757060316

Variant names:

• chr2-219221227-T-A
• NM_001077198.3:c.2221A>T

Your query was ambiguous. Multiple possible variants found:

• chr2-219221227-T-A
• chr2-219221227-T-C
• chr2-219221227-T-G

Variant summary

Our verdict is Uncertain significance. Variant got 4 ACMG points: 4P and 0B. PM1 PM2

The NM_001077198.3(ATG9A):​c.2221A>T​(p.Ser741Cys) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 31)
• Consequence: ATG9A NM_001077198.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 7.40

Genes affected

ATG9A (HGNC:22408): (autophagy related 9A) Acts upstream of or within autophagosome assembly. Located in endosome; phagophore assembly site; and trans-Golgi network. [provided by Alliance of Genome Resources, Apr 2022]

ENSG00000284820 (HGNC:):

ACMG classification

Verdict is Uncertain_significance. Variant got 4 ACMG points.

• PM1: In a modified_residue Phosphoserine (size 0) in uniprot entity ATG9A_HUMAN
• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ATG9A	NM_001077198.3	c.2221A>T	p.Ser741Cys	missense_variant	Exon 14 of 16	ENST00000361242.9	NP_001070666.1
ATG9A	NM_024085.5	c.2221A>T	p.Ser741Cys	missense_variant	Exon 13 of 15		NP_076990.4
ATG9A	NR_104255.2	n.2345A>T		non_coding_transcript_exon_variant	Exon 14 of 16

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ATG9A	ENST00000361242.9	c.2221A>T	p.Ser741Cys	missense_variant	Exon 14 of 16	2	NM_001077198.3	ENSP00000355173.4
ENSG00000284820	ENST00000446716.5	n.466A>T		non_coding_transcript_exon_variant	Exon 4 of 22	2		ENSP00000398528.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 35

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.15
BayesDel_addAF	Uncertain	0.12	D
BayesDel_noAF	Uncertain	-0.070
CADD	Uncertain	25
DANN	Uncertain	0.99
DEOGEN2	Benign	0.14	T;T;T;.
Eigen	Uncertain	0.51
Eigen_PC	Uncertain	0.49
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Uncertain	0.92	.;.;D;D
M_CAP	Uncertain	0.096	D
MetaRNN	Uncertain	0.58	D;D;D;D
MetaSVM	Uncertain	-0.18	T
MutationAssessor	Benign	2.0	M;M;M;.
PrimateAI	Uncertain	0.68	T
PROVEAN	Benign	-1.6	N;N;N;N
REVEL	Uncertain	0.30
Sift	Uncertain	0.0030	D;D;D;D
Sift4G	Uncertain	0.034	D;D;D;D
Polyphen		1.0	D;D;D;.
Vest4		0.68
MutPred		0.17		Loss of phosphorylation at S741 (P = 0.0068);Loss of phosphorylation at S741 (P = 0.0068);Loss of phosphorylation at S741 (P = 0.0068);.;
MVP		0.38
MPC		0.74
ClinPred		0.90	D
GERP RS		5.3
Varity_R		0.28
gMVP		0.47

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: chr2-220085949;