rs137853051

Positions:

• chr1-7965348-G-A
• chr1-7965348-G-T

Variant summary

Our verdict is Uncertain significance. Variant got 2 ACMG points: 4P and 2B. PM2 PM5 BP4_Moderate

The NM_007262.5(PARK7):​c.115G>A​(p.Ala39Thr) 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. 16/21 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. A39S) has been classified as Pathogenic.

• Frequency: Genomes: not found (cov: 32)
• Consequence: PARK7 NM_007262.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.331

Genes affected

PARK7 (HGNC:16369): (Parkinsonism associated deglycase) The product of this gene belongs to the peptidase C56 family of proteins. It acts as a positive regulator of androgen receptor-dependent transcription. It may also function as a redox-sensitive chaperone, as a sensor for oxidative stress, and it apparently protects neurons against oxidative stress and cell death. Defects in this gene are the cause of autosomal recessive early-onset Parkinson disease 7. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PM5: Other missense variant is known to change same aminoacid residue: Variant chr1-7965348-G-T is described in ClinVar as [Pathogenic]. Clinvar id is 7069.Status of the report is no_assertion_criteria_provided, 0 stars.
• BP4: Computational evidence support a benign effect (MetaRNN=0.083305866).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PARK7	NM_007262.5	c.115G>A	p.Ala39Thr	missense_variant	3/7	ENST00000338639.10
PARK7	NM_001123377.2	c.115G>A	p.Ala39Thr	missense_variant	3/7
PARK7	XM_005263424.4	c.115G>A	p.Ala39Thr	missense_variant	3/7

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PARK7	ENST00000338639.10	c.115G>A	p.Ala39Thr	missense_variant	3/7	1	NM_007262.5	P1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

Bravo AF: 0.00000756

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.072
BayesDel_addAF	Benign	-0.19	T
BayesDel_noAF	Benign	-0.51
CADD	Benign	12
DANN	Benign	0.66
DEOGEN2	Benign	0.20	T;T;T;T;T;T
Eigen	Benign	-1.0
Eigen_PC	Benign	-0.88
FATHMM_MKL	Benign	0.72	D
LIST_S2	Benign	0.75	.;.;.;T;.;T
M_CAP	Benign	0.013	T
MetaRNN	Benign	0.083	T;T;T;T;T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	0.65	N;N;N;.;N;N
MutationTaster	Benign	0.95	D;D;D;D;D
PrimateAI	Benign	0.36	T
PROVEAN	Benign	0.46	.;N;N;.;N;N
REVEL	Benign	0.066
Sift	Benign	0.77	.;T;T;.;T;T
Sift4G	Benign	0.73	T;T;T;T;T;T
Polyphen		0.0	B;B;B;.;B;B
Vest4		0.23, 0.19, 0.18
MutPred		0.43		Gain of phosphorylation at A39 (P = 0.0681);Gain of phosphorylation at A39 (P = 0.0681);Gain of phosphorylation at A39 (P = 0.0681);Gain of phosphorylation at A39 (P = 0.0681);Gain of phosphorylation at A39 (P = 0.0681);Gain of phosphorylation at A39 (P = 0.0681);
MVP		0.43
MPC		0.12
ClinPred		0.042	T
GERP RS		-2.1
RBP_binding_hub_radar		0.92
RBP_regulation_power_radar		2.7
Varity_R		0.11
gMVP		0.35

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: rs137853051; hg19: chr1-8025408;