rs1064795494

Positions:

• chr12-6939139-C-CGAACCT
• chr12-6939139-C-CGGACCT

Variant summary

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

The NM_001940.4(ATN1):​c.3177_3178insAACCTG​(p.Ser1059_His1060insAsnLeu) variant causes a inframe insertion change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Uncertain significance (★). Synonymous variant affecting the same amino acid position (i.e. S1059S) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 33)
• Consequence: ATN1 NM_001940.4 inframe_insertion
• Clinical Significance: Uncertain significance criteria provided, single submitter P:1 U:1
• Conservation: PhyloP100: -1.04

Genes affected

ATN1 (HGNC:3033): (atrophin 1) Dentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion from 7-35 copies to 49-93 copies of a trinucleotide repeat (CAG/CAA) within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein. [provided by RefSeq, Jul 2016]

ACMG classification

Verdict is Uncertain_significance. Variant got 4 ACMG points.

• PM1: In a hotspot region, there are 7 aminoacids with missense pathogenic changes in the window of +-8 aminoacids around while only 0 benign, 3 uncertain in NM_001940.4
• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ATN1	NM_001940.4	c.3177_3178insAACCTG	p.Ser1059_His1060insAsnLeu	inframe_insertion	7/10	ENST00000396684.3
ATN1	NM_001007026.2	c.3177_3178insAACCTG	p.Ser1059_His1060insAsnLeu	inframe_insertion	7/10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ATN1	ENST00000396684.3	c.3177_3178insAACCTG	p.Ser1059_His1060insAsnLeu	inframe_insertion	7/10	1	NM_001940.4	P1
ATN1	ENST00000356654.8	c.3177_3178insAACCTG	p.Ser1059_His1060insAsnLeu	inframe_insertion	7/10	1		P1
ATN1	ENST00000537488.1	n.34_35insAACCTG		non_coding_transcript_exon_variant	1/3	2

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 33

GnomAD4 genome Cov.: 33

ClinVar

Significance: Uncertain significance

Submissions summary: Pathogenic:1 Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

Congenital hypotonia, epilepsy, developmental delay, and digital anomalies Pathogenic:1

Pathogenic, no assertion criteria provided

literature only

OMIM

Jul 12, 2019

- -

not provided Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

GeneDx

Aug 18, 2016

The c.3177_3178insAACCTG variant in the ATN1 gene has not been reported previously as apathogenic variant, nor as a benign variant, to our knowledge. The c.3177_3178insAACCTG variant was not observed inapproximately 6500 individuals of European and African American ancestry in the NHLBI ExomeSequencing Project, indicating it is not a common benign variant in these populations. We interpretc.3177_3178insAACCTG as a variant of uncertain significance. -

Computational scores

Source: dbNSFP v4.3

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs1064795494; hg19: chr12-7048302;