10-45826078-C-G

Variant names:

• chr10-45826078-C-G
• NM_001276343.3:c.1898G>C

Variant summary

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

The NM_001276343.3(AGAP4):​c.1898G>C​(p.Arg633Pro) 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. 11/19 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 17)
• Consequence: AGAP4 NM_001276343.3 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: -0.00400

Genes affected

AGAP4 (HGNC:23459): (ArfGAP with GTPase domain, ankyrin repeat and PH domain 4) Predicted to enable GTPase activator activity and metal ion binding activity. Predicted to be involved in regulation of catalytic activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

PARGP1-AGAP4 (HGNC:):

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=0.22920609).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
AGAP4	NM_001276343.3	c.1898G>C	p.Arg633Pro	missense_variant	Exon 8 of 8	ENST00000616763.6	NP_001263272.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
AGAP4	ENST00000616763.6	c.1898G>C	p.Arg633Pro	missense_variant	Exon 8 of 8	1	NM_001276343.3	ENSP00000483751.2
AGAP4	ENST00000448048.7	c.1829G>C	p.Arg610Pro	missense_variant	Exon 7 of 7	1		ENSP00000392513.2

Frequencies

GnomAD3 genomes Cov.: 17

GnomAD4 exome Cov.: 24

GnomAD4 genome Cov.: 17

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

May 24, 2024

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The c.1829G>C (p.R610P) alteration is located in exon 7 (coding exon 7) of the AGAP4 gene. This alteration results from a G to C substitution at nucleotide position 1829, causing the arginine (R) at amino acid position 610 to be replaced by a proline (P). 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	Pathogenic	0.71
BayesDel_addAF	Benign	-0.012	T
BayesDel_noAF	Benign	-0.25
CADD	Benign	20
DANN	Benign	0.92
DEOGEN2	Benign	0.046	T;.;.;.
Eigen	Benign	-0.33
Eigen_PC	Benign	-0.64
FATHMM_MKL	Benign	0.051	N
LIST_S2	Uncertain	0.96	D;D;D;D
M_CAP	Benign	0.0095	T
MetaRNN	Benign	0.23	T;T;T;T
MetaSVM	Benign	-0.36	T
MutationAssessor	Pathogenic	3.3	M;.;.;.
PrimateAI	Uncertain	0.58	T
PROVEAN	Uncertain	-3.2	D;.;.;.
REVEL	Uncertain	0.30
Sift	Benign	0.082	T;.;.;.
Sift4G	Benign	0.21	T;T;T;T
Polyphen		1.0	D;.;.;.
Vest4		0.40
MVP		0.27
ClinPred		0.95	D
Varity_R		0.93
gMVP		0.45

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: chr10-46321526;