chr1-155610437-G-C
Variant summary
Our verdict is Likely benign. Variant got -2 ACMG points: 0P and 2B. BP4_Moderate
The NM_018116.4(MSTO1):c.97G>C(p.Gly33Arg) variant causes a missense change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. 14/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Genomes: 𝑓 0.000065 ( 0 hom., cov: 21)
Exomes 𝑓: 0.000063 ( 0 hom. )
Failed GnomAD Quality Control
Consequence
MSTO1
NM_018116.4 missense
NM_018116.4 missense
Scores
2
11
Clinical Significance
Conservation
PhyloP100: 0.675
Genes affected
MSTO1 (HGNC:29678): (misato mitochondrial distribution and morphology regulator 1) Involved in mitochondrion distribution. Located in cytosol and mitochondrial outer membrane. [provided by Alliance of Genome Resources, Apr 2022]
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ACMG classification
Classification made for transcript
Verdict is Likely_benign. Variant got -2 ACMG points.
BP4
?
Computational evidence support a benign effect (MetaRNN=0.11343381).
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
MSTO1 | NM_018116.4 | c.97G>C | p.Gly33Arg | missense_variant | 2/14 | ENST00000245564.8 | |
LOC105371452 | XR_922171.2 | n.77-545C>G | intron_variant, non_coding_transcript_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
MSTO1 | ENST00000245564.8 | c.97G>C | p.Gly33Arg | missense_variant | 2/14 | 1 | NM_018116.4 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.00 AC: 9AN: 138042Hom.: 0 Cov.: 21 FAILED QC
GnomAD3 genomes
?
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FAILED QC
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GnomAD3 exomes AF: 0.0000581 AC: 5AN: 86018Hom.: 0 AF XY: 0.0000225 AC XY: 1AN XY: 44358
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GnomAD4 exome Data not reliable, filtered out with message: AS_VQSR AF: 0.0000631 AC: 46AN: 728802Hom.: 0 Cov.: 10 AF XY: 0.0000534 AC XY: 20AN XY: 374598
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GnomAD4 genome ? Data not reliable, filtered out with message: AS_VQSR AF: 0.0000652 AC: 9AN: 138042Hom.: 0 Cov.: 21 AF XY: 0.0000452 AC XY: 3AN XY: 66434
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ClinVar
Significance: Uncertain significance
Submissions summary: Uncertain:1
Revision: criteria provided, single submitter
LINK: link
Submissions by phenotype
Inborn genetic diseases Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Aug 17, 2021 | The c.97G>C (p.G33R) alteration is located in exon 2 (coding exon 2) of the MSTO1 gene. This alteration results from a G to C substitution at nucleotide position 97, causing the glycine (G) at amino acid position 33 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. - |
Computational scores
Source:
Name
Calibrated prediction
Score
Prediction
AlphaMissense
Benign
BayesDel_addAF
Benign
T
BayesDel_noAF
Benign
Cadd
Benign
Dann
Uncertain
Eigen
Benign
Eigen_PC
Benign
FATHMM_MKL
Benign
N
LIST_S2
Benign
T;T;T
M_CAP
Benign
T
MetaRNN
Benign
T;T;T
MetaSVM
Benign
T
MutationTaster
Benign
N;N;N;N
PrimateAI
Uncertain
T
Polyphen
0.0030
.;B;.
Vest4
0.099, 0.11
MutPred
Gain of MoRF binding (P = 0.0561);Gain of MoRF binding (P = 0.0561);Gain of MoRF binding (P = 0.0561);
MVP
0.43
MPC
2.1
ClinPred
T
GERP RS
Varity_R
gMVP
Splicing
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SpliceAI score (max)
Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at