1-20651801-T-TTTTTTTTTTTTATTTATTTA

Variant summary

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

The NM_005216.5(DDOST):c.*577_*578insTAAATAAATAAAAAAAAAAA variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency:
  • Genomes: 𝑓 0.0062 (5 hom., cov: 0)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: DDOST NM_005216.5 3_prime_UTR
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 0.118

Genes affected

DDOST (HGNC:2728): (dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit) This gene encodes a component of the oligosaccharyltransferase complex which catalyzes the transfer of high-mannose oligosaccharides to asparagine residues on nascent polypeptides in the lumen of the rough endoplasmic reticulum. The protein complex co-purifies with ribosomes. The product of this gene is also implicated in the processing of advanced glycation endproducts (AGEs), which form from non-enzymatic reactions between sugars and proteins or lipids and are associated with aging and hyperglycemia. [provided by RefSeq, Jul 2008]

PINK1-AS (HGNC:38872): (PINK1 antisense RNA)

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
DDOST	NM_005216.5	c.*577_*578insTAAATAAATAAAAAAAAAAA		3_prime_UTR_variant	11/11	ENST00000602624.7
PINK1-AS	NR_046507.1	n.392_393insTAAATAAATAAAAAAAAAAA		non_coding_transcript_exon_variant	1/3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
DDOST	ENST00000602624.7	c.*577_*578insTAAATAAATAAAAAAAAAAA		3_prime_UTR_variant	11/11	1	NM_005216.5	P1
DDOST	ENST00000415136.6	c.*577_*578insTAAATAAATAAAAAAAAAAA		3_prime_UTR_variant	11/11	1
PINK1-AS	ENST00000451424.1	n.392_393insTAAATAAATAAAAAAAAAAA		non_coding_transcript_exon_variant	1/3	2

Frequencies

GnomAD3 genomes AF: 0.00 AC: 915 AN: 147068 Hom.: 5 Cov.: 0 FAILED QC

Gnomad AFR AF: 0.00191

Gnomad AMI AF: 0.0122

Gnomad AMR AF: 0.00231

Gnomad ASJ AF: 0.00261

Gnomad EAS AF: 0.00343

Gnomad SAS AF: 0.00244

Gnomad FIN AF: 0.00288

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0108

Gnomad OTH AF: 0.00297

GnomAD4 exome Data not reliable, filtered out with message: AC0;AS_VQSR AF: 0.00 AC: 0 AN: 8 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 8

Gnomad4 NFE exome AF: 0.00

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Data not reliable, filtered out with message: AS_VQSR AF: 0.00621 AC: 914 AN: 147158 Hom.: 5 Cov.: 0 AF XY: 0.00536 AC XY: 383 AN XY: 71436

Gnomad4 AFR AF: 0.00191

Gnomad4 AMR AF: 0.00230

Gnomad4 ASJ AF: 0.00261

Gnomad4 EAS AF: 0.00344

Gnomad4 SAS AF: 0.00222

Gnomad4 FIN AF: 0.00288

Gnomad4 NFE AF: 0.0108

Gnomad4 OTH AF: 0.00294

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

Congenital disorder of glycosylation Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Illumina Laboratory Services, Illumina

Jun 14, 2016

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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: rs886045853; hg19: chr1-20978294;