chr21-25592951-A-G
Variant summary
Our verdict is Uncertain significance. Variant got 2 ACMG points: 2P and 0B. PM2
The NM_017446.4(MRPL39):c.782T>C(p.Ile261Thr) variant causes a missense change. The variant allele was found at a frequency of 0.0000652 in 1,611,624 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Uncertain significance (★).
Frequency
Genomes: 𝑓 0.000039 ( 0 hom., cov: 32)
Exomes 𝑓: 0.000068 ( 0 hom. )
Consequence
MRPL39
NM_017446.4 missense
NM_017446.4 missense
Scores
1
10
8
Clinical Significance
Conservation
PhyloP100: 6.08
Genes affected
MRPL39 (HGNC:14027): (mitochondrial ribosomal protein L39) Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein. Two transcript variants encoding distinct isoforms have been described. A pseudogene corresponding to this gene is found on chromosome 5q. [provided by RefSeq, Jul 2008]
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ACMG classification
Classification made for transcript
Verdict is Uncertain_significance. Variant got 2 ACMG points.
PM2
?
Very rare variant in population databases, with high coverage;
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
MRPL39 | NM_017446.4 | c.782T>C | p.Ile261Thr | missense_variant | 8/10 | ENST00000352957.9 | |
MRPL39 | NM_080794.4 | c.782T>C | p.Ile261Thr | missense_variant | 8/11 | ||
MRPL39 | XM_006724026.5 | c.782T>C | p.Ile261Thr | missense_variant | 8/10 | ||
MRPL39 | XM_011529651.3 | c.656T>C | p.Ile219Thr | missense_variant | 8/10 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
MRPL39 | ENST00000352957.9 | c.782T>C | p.Ile261Thr | missense_variant | 8/10 | 1 | NM_017446.4 | P1 | |
MRPL39 | ENST00000307301.11 | c.782T>C | p.Ile261Thr | missense_variant | 8/11 | 5 | |||
MRPL39 | ENST00000419219.1 | c.752T>C | p.Ile251Thr | missense_variant | 8/8 | 5 |
Frequencies
GnomAD3 genomes ? AF: 0.0000394 AC: 6AN: 152200Hom.: 0 Cov.: 32
GnomAD3 genomes
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GnomAD3 exomes AF: 0.0000282 AC: 7AN: 248272Hom.: 0 AF XY: 0.0000298 AC XY: 4AN XY: 134146
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GnomAD4 exome AF: 0.0000678 AC: 99AN: 1459424Hom.: 0 Cov.: 32 AF XY: 0.0000634 AC XY: 46AN XY: 726000
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GnomAD4 genome ? AF: 0.0000394 AC: 6AN: 152200Hom.: 0 Cov.: 32 AF XY: 0.0000672 AC XY: 5AN XY: 74358
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ClinVar
Significance: Uncertain significance
Submissions summary: Uncertain:1
Revision: criteria provided, single submitter
LINK: link
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Jun 13, 2023 | The c.782T>C (p.I261T) alteration is located in exon 8 (coding exon 8) of the MRPL39 gene. This alteration results from a T to C substitution at nucleotide position 782, causing the isoleucine (I) at amino acid position 261 to be replaced by a threonine (T). 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
Pathogenic
Dann
Uncertain
DEOGEN2
Benign
T;.;T
Eigen
Uncertain
Eigen_PC
Uncertain
FATHMM_MKL
Pathogenic
D
LIST_S2
Uncertain
D;D;D
M_CAP
Benign
T
MetaRNN
Uncertain
T;T;T
MetaSVM
Benign
T
MutationAssessor
Benign
M;M;.
MutationTaster
Benign
D;D
PrimateAI
Uncertain
T
PROVEAN
Uncertain
D;D;D
REVEL
Uncertain
Sift
Uncertain
D;D;D
Sift4G
Uncertain
D;D;D
Polyphen
D;D;.
Vest4
MVP
MPC
0.054
ClinPred
D
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