19-9566802-T-G
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2BP4_Moderate
The NM_001008727.5(ZNF121):āc.311A>Cā(p.Gln104Pro) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000372 in 1,614,088 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 13/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (ā ).
Frequency
Consequence
NM_001008727.5 missense
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Uncertain_significance. Variant got 0 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
ZNF121 | NM_001008727.5 | c.311A>C | p.Gln104Pro | missense_variant | 4/4 | ENST00000320451.7 | |
ZNF121 | NM_001308269.3 | c.311A>C | p.Gln104Pro | missense_variant | 5/5 | ||
ZNF121 | XM_017027239.2 | c.311A>C | p.Gln104Pro | missense_variant | 5/5 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
ZNF121 | ENST00000320451.7 | c.311A>C | p.Gln104Pro | missense_variant | 4/4 | 3 | NM_001008727.5 | P1 | |
ZNF121 | ENST00000586602.5 | c.311A>C | p.Gln104Pro | missense_variant | 6/6 | 2 | P1 | ||
ZNF121 | ENST00000591447.1 | c.311A>C | p.Gln104Pro | missense_variant | 2/2 | 3 |
Frequencies
GnomAD3 genomes AF: 0.0000131 AC: 2AN: 152212Hom.: 0 Cov.: 32
GnomAD4 exome AF: 0.00000274 AC: 4AN: 1461876Hom.: 0 Cov.: 31 AF XY: 0.00000138 AC XY: 1AN XY: 727236
GnomAD4 genome AF: 0.0000131 AC: 2AN: 152212Hom.: 0 Cov.: 32 AF XY: 0.00 AC XY: 0AN XY: 74368
ClinVar
Not reported inComputational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at