chrX-11118538-A-G

Position:

• chrX-11118538-A-G

Variant summary

Our verdict is Uncertain significance. Variant got 4 ACMG points: 4P and 0B. PM2 PP3_Moderate

The NM_005333.5(HCCS):​c.439A>G​(p.Met147Val) 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 Uncertain significance (★).

• Frequency: Genomes: not found (cov: 23)
• Consequence: HCCS NM_005333.5 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 8.72

Genes affected

HCCS (HGNC:4837): (holocytochrome c synthase) The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]

ARHGAP6 (HGNC:676): (Rho GTPase activating protein 6) This gene encodes a member of the rhoGAP family of proteins which play a role in the regulation of actin polymerization at the plasma membrane during several cellular processes. This protein is thought to have two independent functions, one as a GTPase-activating protein with specificity for RhoA, and another as a cytoskeletal protein that promotes actin remodeling. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 4 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.868

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
HCCS	NM_005333.5	c.439A>G	p.Met147Val	missense_variant	5/7	ENST00000380762.5	NP_005324.3
HCCS	NM_001122608.3	c.439A>G	p.Met147Val	missense_variant	5/7		NP_001116080.1
HCCS	NM_001171991.3	c.439A>G	p.Met147Val	missense_variant	5/7		NP_001165462.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
HCCS	ENST00000380762.5	c.439A>G	p.Met147Val	missense_variant	5/7	1	NM_005333.5	ENSP00000370139	P1
HCCS	ENST00000380763.7	c.439A>G	p.Met147Val	missense_variant	5/7	1		ENSP00000370140	P1
HCCS	ENST00000321143.8	c.439A>G	p.Met147Val	missense_variant	5/7	2		ENSP00000326579	P1
ARHGAP6	ENST00000657361.1	c.1784-179T>C		intron_variant				ENSP00000499351	A2

Frequencies

GnomAD3 genomes Cov.: 23

GnomAD4 exome Cov.: 25

GnomAD4 genome Cov.: 23

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

HCCS-related disorder Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

PreventionGenetics, part of Exact Sciences

Feb 23, 2023

The HCCS c.439A>G variant is predicted to result in the amino acid substitution p.Met147Val. To our knowledge, this variant has not been reported in the literature or in a large population database (http://gnomad.broadinstitute.org), indicating this variant is rare. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.27
BayesDel_addAF	Pathogenic	0.42	D
BayesDel_noAF	Pathogenic	0.37
CADD	Benign	23
DANN	Benign	0.97
DEOGEN2	Uncertain	0.74	D;D;D
FATHMM_MKL	Pathogenic	0.99	D
LIST_S2	Uncertain	0.93	.;.;D
M_CAP	Pathogenic	0.49	D
MetaRNN	Pathogenic	0.87	D;D;D
MetaSVM	Benign	-0.34	T
MutationAssessor	Benign	1.2	L;L;L
MutationTaster	Benign	1.0	D;D;D;D
PrimateAI	Uncertain	0.66	T
PROVEAN	Uncertain	-3.9	D;D;D
REVEL	Pathogenic	0.69
Sift	Benign	0.063	T;T;T
Sift4G	Uncertain	0.048	D;D;D
Polyphen		0.13	B;B;B
Vest4		0.71
MutPred		0.59		Loss of ubiquitination at K145 (P = 0.058);Loss of ubiquitination at K145 (P = 0.058);Loss of ubiquitination at K145 (P = 0.058);
MVP		0.94
MPC		0.50
ClinPred		0.91	D
GERP RS		5.6
Varity_R		0.63
gMVP		0.96

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: chrX-11136658;