rs79556186
Variant summary
Our verdict is Uncertain significance. The variant received 2 ACMG points: 2P and 0B. PM2
The NM_001083614.2(EARS2):c.*1901_*1902delAA variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Consequence
NM_001083614.2 3_prime_UTR
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Uncertain_significance. The variant received 2 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_001083614.2. You can select a different transcript below to see updated ACMG assignments.
RefSeq Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| EARS2 | NM_001083614.2 | MANE Select | c.*1901_*1902delAA | 3_prime_UTR | Exon 9 of 9 | NP_001077083.1 | Q5JPH6-1 | ||
| EARS2 | NR_003501.2 | n.3387_3388delAA | non_coding_transcript_exon | Exon 10 of 10 |
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| EARS2 | ENST00000449606.7 | TSL:1 MANE Select | c.*1901_*1902delAA | 3_prime_UTR | Exon 9 of 9 | ENSP00000395196.2 | Q5JPH6-1 | ||
| EARS2 | ENST00000674054.1 | n.*1808_*1809delAA | non_coding_transcript_exon | Exon 10 of 10 | ENSP00000501251.1 | Q5JPH6-1 | |||
| EARS2 | ENST00000674054.1 | n.*1808_*1809delAA | 3_prime_UTR | Exon 10 of 10 | ENSP00000501251.1 | Q5JPH6-1 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0AN: 72Hom.: 0 AF XY: 0.00 AC XY: 0AN XY: 40
GnomAD4 genome Cov.: 32
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at