chr14-51094459-T-C
Variant summary
Our verdict is Likely benign. Variant got -2 ACMG points: 0P and 2B. BP4_Moderate
The NM_001387360.1(TRIM9):c.481A>G(p.Ser161Gly) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000889 in 1,461,504 control chromosomes in the GnomAD database, with no homozygous occurrence. 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
Consequence
NM_001387360.1 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_benign. Variant got -2 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
TRIM9 | NM_001387360.1 | c.481A>G | p.Ser161Gly | missense_variant | 1/13 | ENST00000684578.1 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
TRIM9 | ENST00000684578.1 | c.481A>G | p.Ser161Gly | missense_variant | 1/13 | NM_001387360.1 | |||
TRIM9 | ENST00000298355.7 | c.481A>G | p.Ser161Gly | missense_variant | 1/10 | 1 | P1 | ||
TRIM9 | ENST00000360392.4 | c.481A>G | p.Ser161Gly | missense_variant | 1/7 | 1 | |||
TRIM9 | ENST00000338969.9 | c.481A>G | p.Ser161Gly | missense_variant | 1/12 | 2 |
Frequencies
GnomAD3 genomes ? Cov.: 33
GnomAD3 exomes AF: 0.0000120 AC: 3AN: 250042Hom.: 0 AF XY: 0.0000148 AC XY: 2AN XY: 135516
GnomAD4 exome AF: 0.00000889 AC: 13AN: 1461504Hom.: 0 Cov.: 31 AF XY: 0.00000963 AC XY: 7AN XY: 727064
GnomAD4 genome ? Cov.: 33
ClinVar
Submissions by phenotype
not specified Uncertain:1
Uncertain significance, criteria provided, single submitter | clinical testing | Ambry Genetics | Jul 20, 2021 | The c.481A>G (p.S161G) alteration is located in exon 1 (coding exon 1) of the TRIM9 gene. This alteration results from a A to G substitution at nucleotide position 481, causing the serine (S) at amino acid position 161 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at