chr6-152323532-C-A

Variant names:

• chr6-152323532-C-A
• NM_182961.4:c.15863G>T

Variant summary

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

The NM_182961.4(SYNE1):​c.15863G>T​(p.Gly5288Val) 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. 14/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 33)
• Consequence: SYNE1 NM_182961.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.490

Genes affected

SYNE1 (HGNC:17089): (spectrin repeat containing nuclear envelope protein 1) This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

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=0.095924735).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SYNE1	NM_182961.4	c.15863G>T	p.Gly5288Val	missense_variant	Exon 82 of 146	ENST00000367255.10	NP_892006.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SYNE1	ENST00000367255.10	c.15863G>T	p.Gly5288Val	missense_variant	Exon 82 of 146	1	NM_182961.4	ENSP00000356224.5
SYNE1	ENST00000423061.6	c.15650G>T	p.Gly5217Val	missense_variant	Exon 81 of 146	1		ENSP00000396024.1
SYNE1	ENST00000490135.6	n.3209G>T		non_coding_transcript_exon_variant	Exon 6 of 11	1

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.090
BayesDel_addAF	Benign	-0.25	T
BayesDel_noAF	Benign	-0.59
CADD	Benign	5.9
DANN	Benign	0.53
DEOGEN2	Benign	0.16	T;.;T
Eigen	Benign	-0.71
Eigen_PC	Benign	-0.69
FATHMM_MKL	Benign	0.34	N
LIST_S2	Uncertain	0.86	D;D;T
M_CAP	Benign	0.014	T
MetaRNN	Benign	0.096	T;T;T
MetaSVM	Benign	-1.1	T
MutationAssessor	Uncertain	2.5	M;.;.
PrimateAI	Benign	0.29	T
PROVEAN	Benign	-0.78	N;.;N
REVEL	Benign	0.012
Sift	Benign	0.43	T;.;T
Sift4G	Benign	0.32	T;T;T
Polyphen		0.037	B;.;.
Vest4		0.24
MutPred		0.24		Loss of glycosylation at P5287 (P = 0.0601);.;.;
MVP		0.34
MPC		0.18
ClinPred		0.087	T
GERP RS		3.2
Varity_R		0.031
gMVP		0.089

Splicing

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: chr6-152644667;