chr16-3026176-C-T
Variant summary
Our verdict is Likely benign. Variant got -4 ACMG points: 2P and 6B. PM2BP4_StrongBP6_Moderate
The NM_024339.5(THOC6):c.324+10C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000176 in 1,611,198 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).
Frequency
Genomes: 𝑓 0.00012 ( 0 hom., cov: 33)
Exomes 𝑓: 0.00018 ( 0 hom. )
Consequence
THOC6
NM_024339.5 intron
NM_024339.5 intron
Scores
2
Clinical Significance
Conservation
PhyloP100: -0.541
Genes affected
THOC6 (HGNC:28369): (THO complex subunit 6) This gene encodes a subunit of the multi-protein THO complex, which is involved in coordination between transcription and mRNA processing. The THO complex is a component of the TREX (transcription/export) complex, which is involved in transcription and export of mRNAs. A missense mutation in this gene is associated with a neurodevelopmental disorder called Beaulieu-Boycott-Innes syndrome. [provided by RefSeq, Dec 2016]
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ACMG classification
Classification made for transcript
Verdict is Likely_benign. Variant got -4 ACMG points.
PM2
?
Very rare variant in population databases, with high coverage;
BP4
?
Computational evidence support a benign effect (BayesDel_noAF=-0.85).
BP6
?
Variant 16-3026176-C-T is Benign according to our data. Variant chr16-3026176-C-T is described in ClinVar as [Likely_benign]. Clinvar id is 727901.Status of the report is criteria_provided_single_submitter, 1 stars.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
THOC6 | NM_024339.5 | c.324+10C>T | intron_variant | ENST00000326266.13 | |||
THOC6 | NM_001142350.3 | c.324+10C>T | intron_variant | ||||
THOC6 | NM_001347703.2 | c.252+10C>T | intron_variant | ||||
THOC6 | NM_001347704.2 | c.324+10C>T | intron_variant |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
THOC6 | ENST00000326266.13 | c.324+10C>T | intron_variant | 1 | NM_024339.5 | P1 |
Frequencies
GnomAD3 genomes ? AF: 0.000118 AC: 18AN: 152154Hom.: 0 Cov.: 33
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GnomAD3 exomes AF: 0.0000681 AC: 17AN: 249486Hom.: 0 AF XY: 0.0000668 AC XY: 9AN XY: 134768
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GnomAD4 exome AF: 0.000182 AC: 265AN: 1459044Hom.: 0 Cov.: 38 AF XY: 0.000182 AC XY: 132AN XY: 725392
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GnomAD4 genome ? AF: 0.000118 AC: 18AN: 152154Hom.: 0 Cov.: 33 AF XY: 0.000135 AC XY: 10AN XY: 74334
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ClinVar
Significance: Likely benign
Submissions summary: Benign:1
Revision: criteria provided, single submitter
LINK: link
Submissions by phenotype
not provided Benign:1
Likely benign, criteria provided, single submitter | clinical testing | Invitae | May 14, 2018 | - - |
Computational scores
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Name
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BayesDel_noAF
Benign
Cadd
Benign
Dann
Benign
RBP_binding_hub_radar
RBP_regulation_power_radar
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Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at