17-75261927-C-A
Variant summary
Our verdict is Likely benign. The variant received -3 ACMG points: 2P and 5B. PM2BP4_StrongBP7
The NM_015971.4(MRPS7):c.27C>A(p.Ala9Ala) variant causes a synonymous 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Synonymous variant affecting the same amino acid position (i.e. A9A) has been classified as Likely benign.
Frequency
Consequence
NM_015971.4 synonymous
Scores
Clinical Significance
Conservation
Publications
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ACMG classification
Our verdict: Likely_benign. The variant received -3 ACMG points.
Variant Effect in Transcripts
ACMG analysis was done for transcript: NM_015971.4. You can select a different transcript below to see updated ACMG assignments.
Ensembl Transcripts
| Sel. | Gene | Transcript | Tags | HGVSc | HGVSp | Effect | Exon Rank | Protein | UniProt |
|---|---|---|---|---|---|---|---|---|---|
| MRPS7 | TSL:1 MANE Select | c.27C>A | p.Ala9Ala | synonymous | Exon 1 of 5 | ENSP00000245539.6 | Q9Y2R9 | ||
| MRPS7 | c.27C>A | p.Ala9Ala | synonymous | Exon 1 of 6 | ENSP00000556375.1 | ||||
| MRPS7 | c.27C>A | p.Ala9Ala | synonymous | Exon 1 of 6 | ENSP00000582591.1 |
Frequencies
GnomAD3 genomes Cov.: 34
GnomAD4 exome Cov.: 64
GnomAD4 genome Cov.: 34
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at